Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion type Assertion NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_head.
- NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion description "[The LGMD2C linked to chromosome 13q and related to a 35 KDa dystrophin-associated glycoprotein deficiency, is very similar to Duchenne muscular dystrophy with an autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_provenance.
- NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion evidence source_evidence_literature NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_provenance.
- NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion SIO_000772 9027861 NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_provenance.
- NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion wasDerivedFrom befree-20140225 NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_provenance.
- NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_assertion wasGeneratedBy ECO_0000203 NP162439.RACN53jRvyUXngU-rPmdK_cHlrVj3PkPPvugmsa7-kdek130_provenance.