Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_assertion description "[These results show that the APAF1 variants associated with risk for MDD in the Utah pedigrees are very rare in Northern European and European-American populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_assertion evidence source_evidence_literature NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_assertion SIO_000772 19455599 NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_assertion wasDerivedFrom befree-2016 NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_assertion wasGeneratedBy ECO_0000203 NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.
- befree-2016 importedOn "2016-02-19" NP740126.RApiusULMSODwPR15xBSknSQB7gcWHLZrzIipPru0vbfo130_provenance.