Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_assertion description "[Mutations in the type IV collagen gene, COL4A5, are associated with Alport syndrome, characterized by ultrastructural abnormalities of the glomerular basement membrane (GBM), with or without progressive loss of renal function, characteristic ophthalmic signs and/or high tone sensorineural deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_assertion evidence source_evidence_literature NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_assertion SIO_000772 17277342 NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_assertion wasDerivedFrom befree-20150227 NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_assertion wasGeneratedBy ECO_0000203 NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320062.RA0VGnTTkhrsSTshvU8_4JMvlc-Fn0TIw0x6azVrvb7bA130_provenance.