Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_assertion description "[Results of the current study support a causative role for the A1166 C polymorphism of the angiotensin II type 1 gene polymorphism in the pathogenesis or phenotypic expression of polycystic ovary syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_assertion evidence source_evidence_literature NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_assertion SIO_000772 23564192 NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_assertion wasDerivedFrom befree-20150227 NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_assertion wasGeneratedBy ECO_0000203 NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP229280.RAdzcbShkSere-SpgEYAqQ50sa7cV2HdXy2PGAsf9PucQ130_provenance.