Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion type Assertion NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_head.
- NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion description "[All patients with POMT1 and POMT2 mutations had evidence of either structural or functional central nervous system involvement including four patients with mental retardation and a LGMD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_provenance.
- NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion evidence source_evidence_literature NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_provenance.
- NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion SIO_000772 17878207 NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_provenance.
- NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion wasDerivedFrom befree-20140225 NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_provenance.
- NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_assertion wasGeneratedBy ECO_0000203 NP628679.RAPTjxiqkhprZbKU9JibSMkgM48a4QOrgyQTW2nAxY5B0130_provenance.