Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_assertion evidence source_evidence_literature NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_assertion SIO_000772 22184204 NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_assertion wasDerivedFrom befree-20140225 NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_assertion wasGeneratedBy ECO_0000203 NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.