Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_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." NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_assertion evidence source_evidence_curated NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_assertion SIO_000772 10729710 NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_assertion wasDerivedFrom uniprot-20130724 NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_assertion wasGeneratedBy ECO_0000218 NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4968.RACVGS1EuStHn18JGP4_JU3jsscpO7kRDUZcLS_415Q6c130_provenance.