- From: ljgarcia <ljgarcia@ebi.ac.uk>
- Date: Fri, 10 Nov 2017 14:21:16 +0000
- To: "Gray, Alasdair J G" <A.J.G.Gray@hw.ac.uk>
- Cc: public-bioschemas@w3.org
Hi, >> I thought we did not want to impose any IRI. Is there any reason why >> we should? > > But then we sacrifice the interoperability and understanding that we > are striving for. If you look at the n-quads for the two examples > (included at the end of this email) then you will see a different set > of triples. If there are mappings between the terms, that interoperability we want to achieve could still be achieved, could not it? With mappings, we still can transform any n-quads to the, let's say, canonical Bioschemas defined form. Would this not be a way? If a mapping cannot be found, then validation fails. Bioschemas should then use mapping tools and clearly state what the use mappings tool is. Regards, On 2017-11-10 14:07, Gray, Alasdair J G wrote: >> On 10 Nov 2017, at 13:28, Leyla Garcia <ljgarcia@ebi.ac.uk> wrote: >> I was under the same impression than Melanie. We agree on aliases >> but providers can decide what is their preferred IRI for any of >> them. A Bioschemas Protein context would just provide a default >> context that can also be used as a template where IRIs (but not >> aliases) can be modified. And of course, anyone could add more >> aliases, Bioschemas will just not parse those outside the >> default/template provided context. >> >> I thought we did not want to impose any IRI. Is there any reason why >> we should? > > But then we sacrifice the interoperability and understanding that we > are striving for. If you look at the n-quads for the two examples > (included at the end of this email) then you will see a different set > of triples. Aliases are only defined within the document. When you > interpret them they give you different meanings. If we go down this > route, we would need to make our tooling with knowledge of either all > possible terms that will be used or mapping aware. > > Alasdair > > http://tinyurl.com/y9mu423y > > <http://identifiers.org/ncbigene/25> <http://schema.org/name> "ABL1" . > > <http://identifiers.org/ncbigene/25> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://purl.obolibrary.org/obo/SO_0000704> . > <http://identifiers.org/ncbigene/25> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://schema.org/BioChemEntity> . > <http://identifiers.org/uniprot/P00519> > <http://schema.org/alternateName> "ABL" . > <http://identifiers.org/uniprot/P00519> > <http://schema.org/alternateName> "JTK7" . > <http://identifiers.org/uniprot/P00519> > <http://schema.org/description> "Non-receptor tyrosine-protein kinase > that plays a role..." . > <http://identifiers.org/uniprot/P00519> <http://schema.org/name> > "ABL1" . > <http://identifiers.org/uniprot/P00519> > <http://semanticscience.org/resource/SIO_000001> > <http://pfam.xfam.org/clan/CL0001> . > <http://identifiers.org/uniprot/P00519> > <http://semanticscience.org/resource/SIO_010081> > <http://identifiers.org/ncbigene/25> . > <http://identifiers.org/uniprot/P00519> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://purl.obolibrary.org/obo/PR_000000001> . > <http://identifiers.org/uniprot/P00519> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://schema.org/BioChemEntity> . > > http://tinyurl.com/yd5snze2 > > <http://identifiers.org/ncbigene/25> <http://schema.org/name> "ABL1" . > > <http://identifiers.org/ncbigene/25> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://purl.obolibrary.org/obo/OGI_0000004> . > <http://identifiers.org/ncbigene/25> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://schema.org/BioChemEntity> . > <http://identifiers.org/uniprot/P00519> > <http://purl.obolibrary.org/obo/RO_0002510> > <http://identifiers.org/ncbigene/25> . > <http://identifiers.org/uniprot/P00519> > <http://schema.org/alternateName> "ABL" . > <http://identifiers.org/uniprot/P00519> > <http://schema.org/alternateName> "JTK7" . > <http://identifiers.org/uniprot/P00519> > <http://schema.org/description> "Non-receptor tyrosine-protein kinase > that plays a role..." . > <http://identifiers.org/uniprot/P00519> <http://schema.org/name> > "ABL1" . > <http://identifiers.org/uniprot/P00519> > <http://semanticscience.org/resource/SIO_000001> > <http://pfam.xfam.org/clan/CL0001> . > <http://identifiers.org/uniprot/P00519> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://purl.obolibrary.org/obo/NCIT_C17021> . > <http://identifiers.org/uniprot/P00519> > <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> > <http://schema.org/BioChemEntity> . > > Alasdair J G Gray > > Fellow of the Higher Education Academy > Assistant Professor in Computer Science, > School of Mathematical and Computer Sciences > (Athena SWAN Bronze Award) > Heriot-Watt University, Edinburgh UK. > > Email: A.J.G.Gray@hw.ac.uk > Web: http://www.macs.hw.ac.uk/~ajg33 > ORCID: http://orcid.org/0000-0002-5711-4872 > Office: Earl Mountbatten Building 1.39 > Twitter: @gray_alasdair > > Untitled Document .fsize { font-family: Arial, Helvetica Neue, > Helvetica, sans-serif; font-size: 10px; } > > ------------------------- > > _HERIOT-WATT UNIVERSITY IS THE TIMES & THE SUNDAY TIMES INTERNATIONAL > UNIVERSITY OF THE YEAR 2018_ > > Founded in 1821, Heriot-Watt is a leader in ideas and solutions. 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Received on Friday, 10 November 2017 14:21:47 UTC