Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion> ?p ?o ?g. }
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- NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion type Assertion NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_head.
- NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion wasGeneratedBy ECO_0000203 NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_provenance.
- NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion wasDerivedFrom lhgdn-20090331 NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_provenance.
- NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion SIO_000772 15563506 NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_provenance.
- NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion evidence source_evidence_literature NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_provenance.
- NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_assertion description "[dominant mutations are common in Ullrich congenital muscular dystrophy (UCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145083.RArdKKNDm9BvwxHhHRGZp2fHkWjb8ibSexGLfyL-9RKY4130_provenance.