Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion> ?p ?o ?g. }
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- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion type Assertion NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_head.
- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion wasGeneratedBy ECO_0000203 NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_provenance.
- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion wasDerivedFrom befree-20140225 NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_provenance.
- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion SIO_000772 24076603 NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_provenance.
- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion evidence source_evidence_literature NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_provenance.
- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_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." NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_provenance.