Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_assertion> ?p ?o ?g. }
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- NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_assertion type Assertion NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_head.
- NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_assertion wasGeneratedBy ECO_0000203 NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_provenance.
- NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_assertion wasDerivedFrom befree-20150227 NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_provenance.
- NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_assertion SIO_000772 24076603 NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_provenance.
- NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_assertion evidence source_evidence_literature NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_provenance.
- NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_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." NP912029.RABPtkhPxyarLz9NW-X1WYQ3AmhkXD7cDozNMf5JdVIzg130_provenance.