Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion type Assertion NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_head.
- NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion wasGeneratedBy ECO_0000218 NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_provenance.
- NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion wasDerivedFrom uniprot-20150221 NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_provenance.
- NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion SIO_000772 11549681 NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_provenance.
- NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion evidence source_evidence_curated NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_provenance.
- NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-MA1/4llerian type II receptor in a family affected by the persistent MA1/4llerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3741.RAq4yAaPQUDI27mOefvanZlXPHr0vsqTUCwbnkmpaUlGg130_provenance.