Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion> ?p ?o ?g. }
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- NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_assertion type Assertion NP21411.RAaOfFla3SoQdTPyHmLGbsU6By5HfUJYXRHBkhbrsldhM130_head.
- 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.