Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion description "[Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion evidence source_evidence_literature NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion SIO_000772 16542388 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion wasDerivedFrom gad-20150221 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_assertion wasGeneratedBy ECO_0000203 NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99513.RAKUQYLB0L0DvB7je6IEn3oNDsLPfpRU65JyHgnG0C6Vw130_provenance.