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- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion type Assertion NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_head.
- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion wasGeneratedBy ECO_0000203 NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_provenance.
- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion wasDerivedFrom befree-20150227 NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_provenance.
- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion SIO_000772 11549681 NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_provenance.
- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion evidence source_evidence_literature NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_provenance.
- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_provenance.