Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_assertion wasGeneratedBy ECO_0000218 NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_assertion wasDerivedFrom ctd_human-20150221 NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_assertion SIO_000772 24076603 NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_assertion evidence source_evidence_curated NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_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." NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.