Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_assertion description "[Mutations in TRPP2 (polycystin-2) cause autosomal dominant polycystic kidney disease (ADPKD), a common genetic disorder characterized by progressive development of fluid-filled cysts in the kidney and other organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_assertion evidence source_evidence_literature NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_assertion SIO_000772 17292589 NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_assertion wasDerivedFrom befree-2016 NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_assertion wasGeneratedBy ECO_0000203 NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.
- befree-2016 importedOn "2016-02-19" NP593228.RAA0B7p-baawNRR_2OJ7doF6NbbVSn-sS5oBAvlcDZP0A130_provenance.