Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_assertion description "[Mutations in WDR19 encoding the intraflagellar transport component IFT144 have recently been described in single families with the clinically overlapping skeletal ciliopathies Jeune and Sensenbrenner syndromes, combined or isolated nephronophthisis (NPHP) and retinitis pigmentosa (RP) (Senior-Loken syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_assertion evidence source_evidence_literature NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_assertion SIO_000772 24504730 NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_assertion wasDerivedFrom befree-2016 NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_assertion wasGeneratedBy ECO_0000203 NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1153009.RAXft-IXrhtPuOpsVWOaJO-aWkbN22Qsogc-qxS6gKvhs130_provenance.