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- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion type Assertion NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_head.
- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion wasGeneratedBy ECO_0000203 NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_provenance.
- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion wasDerivedFrom befree-2016 NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_provenance.
- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion SIO_000772 24076603 NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_provenance.
- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion evidence source_evidence_literature NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_provenance.
- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_provenance.