Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_assertion description "[Our study replicated previous GWAS findings for markers in VAX1 in the Asian population, and identified rare variants in PAX7 and VAX1 that may contribute to the etiology of CL(P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_assertion evidence source_evidence_literature NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_assertion SIO_000772 23463464 NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_assertion wasDerivedFrom befree-20150227 NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_assertion wasGeneratedBy ECO_0000203 NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP858925.RApK7Q82b7fMMbEhpkCfGY4yE7pPBLtjaZGDkkVSqzEsY130_provenance.