Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_assertion description "[A grandmother with the PKD1 gene mutation in mosaicism (p.Val1105ArgfsX4) and with mild clinical course of ADPKD (end stage renal failure at the age of 77) seemed to have ADPKD because of PKD2 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_assertion evidence source_evidence_literature NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_assertion SIO_000772 23496908 NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_assertion wasDerivedFrom befree-20150227 NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_assertion wasGeneratedBy ECO_0000203 NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP643261.RAn431ghwpAGlRsw5wawz73rKMb3hdcif578arjDD9dL8130_provenance.