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- source_evidence_literature type ECO_0000212 NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_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." NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_assertion evidence source_evidence_literature NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_assertion SIO_000772 23261303 NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_assertion wasDerivedFrom befree-20150227 NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_assertion wasGeneratedBy ECO_0000203 NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_provenance.