Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_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." NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_assertion evidence source_evidence_literature NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_assertion SIO_000772 19331813 NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_assertion wasDerivedFrom befree-20140225 NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_assertion wasGeneratedBy ECO_0000203 NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP460835.RAHmSu8KwOK9KZVK47Q2N8rHH4HsfuleXGE1Ai5TCANVs130_provenance.