Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_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." NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_assertion evidence source_evidence_literature NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_assertion SIO_000772 23496908 NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_assertion wasDerivedFrom befree-2016 NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_assertion wasGeneratedBy ECO_0000203 NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1060698.RAm3afjlDVHI7VRiPZ8kkj3YxKZJhdq5HlrcKxRCOdYvY130_provenance.