Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_assertion description "[From these results, it was concluded that the single amino-acid substitution of V2R is responsible for this familial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_assertion evidence source_evidence_literature NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_assertion SIO_000772 8704106 NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_assertion wasDerivedFrom befree-20140225 NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_assertion wasGeneratedBy ECO_0000203 NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP698596.RAYc7ugrca8I4GQ226Hfij3iiUbaUotISo3kBHUQEJLFY130_provenance.