Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion evidence source_evidence_literature NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion SIO_000772 16916875 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion wasDerivedFrom befree-20140225 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_assertion wasGeneratedBy ECO_0000203 NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316670.RA9SaU2hTp81_ID1XNV98Nket3DtOePswouygxiAU-deM130_provenance.