Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_assertion description "[The autosomal dominant polycystic kidney disease (ADPKD) is mostly caused by mutations in the PKD1 (polycystic kidney disease 1) gene located in 16p13.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_assertion evidence source_evidence_literature NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_assertion SIO_000772 18822117 NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_assertion wasDerivedFrom befree-2016 NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_assertion wasGeneratedBy ECO_0000203 NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.
- befree-2016 importedOn "2016-02-19" NP695307.RA3BZEsRXTVycFzD6lvilzdIWSKEBfDkkG5xnlH8Spnc0130_provenance.