Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_assertion description "[Recently, a large-scale genetic epidemiological study has shown significant association of single nucleotide polymorphisms (SNPs) in the protein kinase C eta (PRKCH) gene with cerebral infarction, particularly, with lacunar infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_assertion evidence source_evidence_literature NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_assertion SIO_000772 18164711 NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_assertion wasDerivedFrom befree-2016 NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_assertion wasGeneratedBy ECO_0000203 NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.
- befree-2016 importedOn "2016-02-19" NP647566.RANS6xl_VsxO1GNLMjh8_bTU-UWCLEd58b9Wjzdm9X0UE130_provenance.