Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_assertion description "[The detection of additional disease-causing PKD1 mutations will help in identifying the location of the important functional regions of polycystin-1 and help us to better understand the pathophysiology of ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_assertion evidence source_evidence_curated NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_assertion SIO_000772 10729710 NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_assertion wasDerivedFrom uniprot-20150221 NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_assertion wasGeneratedBy ECO_0000218 NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3167.RAsHyPKkp_ZgNgggX-1fs0bawxLkAuhffSN6YcsdiK5zI130_provenance.