Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_assertion> ?p ?o ?g. }
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- NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_assertion type Assertion NP962297.RAE_7edxhZvf02lKbmJwmNa_fEv3IhF2LmQlV3M6ysabY130_head.
- 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.