Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_assertion description "[Here, we identify loss-of-function mutations in CCDC114 causing PCD with laterality malformations involving complex heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_assertion evidence source_evidence_literature NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_assertion SIO_000772 23261303 NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_assertion wasDerivedFrom befree-20140225 NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_assertion wasGeneratedBy ECO_0000203 NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP358397.RA0o4ON0q1X2ox95g0q4tqwYor91TKpJ7NMDooUNlsDJE130_provenance.