Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_assertion description "[The HNMT T314 allele was detected in 3.5% of the DU patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_assertion evidence source_evidence_literature NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_assertion SIO_000772 18086566 NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_assertion wasDerivedFrom befree-20140225 NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_assertion wasGeneratedBy ECO_0000203 NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP607695.RA1RxPvQEnyIeltsJcET9T4IJhj3_aL3IJquDGN1dKAIk130_provenance.