Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_assertion description "[Collagen type IV nephropathy is an entity in itself, and phenotypic manifestations of COL4A3/COL4A4 mutations may range from monosymptomatic hematuria (BFH) to severe renal failure (AS), depending on the gene dosage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_assertion evidence source_evidence_literature NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_assertion SIO_000772 14582039 NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_assertion wasDerivedFrom befree-2016 NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_assertion wasGeneratedBy ECO_0000203 NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.
- befree-2016 importedOn "2016-02-19" NP418457.RAf2Y3NVMWRNaq5v9LMsi6KerYGor0hEN0GmYnr3YI1mU130_provenance.