Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_assertion description "[It further suggests that WDR19 mutations can cause a broad spectrum of ciliopathies that extends to Jeune and Sensenbrenner syndromes, RP and renal NPHP-like phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_assertion evidence source_evidence_literature NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_assertion SIO_000772 24504730 NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_assertion wasDerivedFrom befree-2016 NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_assertion wasGeneratedBy ECO_0000203 NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1153011.RAXQhmtNr3raZoQJAUs1BnEZ8539Pru4XE8lCzqsP9kDo130_provenance.