Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_assertion wasGeneratedBy ECO_0000203 NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_assertion wasDerivedFrom befree-2016 NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_assertion SIO_000772 24398087 NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_assertion evidence source_evidence_literature NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.
- NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_assertion description "[Collagen type IV related nephropathies are due to the defects in collagen IV genes COL4A3, COL4A4, or COL4A5 and comprise a spectrum of phenotypes ranging from Alport Syndrome (AS) to its mild variants, termed as familial haematuria or thin basement membrane nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1142691.RAkTDBWGo9Qt1DiE1ohKe6FUlbxG1Gw378V2zmafjujF0130_provenance.