Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion wasGeneratedBy ECO_0000218 NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion wasDerivedFrom ctd_human-20150221 NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion SIO_000772 24076603 NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion evidence source_evidence_curated NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.
- NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion description "[Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_provenance.