Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_assertion description "[Moreover, at least 40% of benign familial hematuria (BFH) cases cosegregate with the COL4A3/COL4A4 loci, following a dominant pattern of inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_assertion evidence source_evidence_literature NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_assertion SIO_000772 14582039 NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_assertion wasDerivedFrom befree-20150227 NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_assertion wasGeneratedBy ECO_0000203 NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319883.RAje_faXWXRUIaWH1SrVDCQ-xzNdRBBxJZJ9dGdcHeCLo130_provenance.