Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_assertion type Assertion NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_head.
- NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_assertion wasGeneratedBy ECO_0000203 NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_provenance.
- NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_assertion wasDerivedFrom lhgdn-20090331 NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_provenance.
- NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_assertion SIO_000772 15563506 NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_provenance.
- NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_assertion evidence source_evidence_literature NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_provenance.
- NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_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." NP207963.RAUNSU1jXAzqOlY0yAxNnFalDQNmaD6ndYrvjWtTiFfak130_provenance.