Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_assertion description "[Mutations of PKD1 cause autosomal dominant polycystic kidney disease (ADPKD), a syndrome characterized by kidney cysts and progressive renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_assertion evidence source_evidence_literature NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_assertion SIO_000772 19331813 NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_assertion wasDerivedFrom befree-20140225 NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_assertion wasGeneratedBy ECO_0000203 NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP547317.RAFPbo_12gcsS6tRzMoq4V4PpI8XS95geGxqRP8wFBJ_o130_provenance.