Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion type Assertion NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_head.
- NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion description "[FHL1 mutations cause Emery-Dreifuss muscular dystrophy (OMIM 310300), X-linked myopathy with postural muscle atrophy (XMPMA, OMIM 300696), scapuloperoneal myopathy (OMIM 300695), or reducing body myopathy (OMIM 300717, 300718).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_provenance.
- NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion evidence source_evidence_literature NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_provenance.
- NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion SIO_000772 21932316 NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_provenance.
- NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion wasDerivedFrom befree-2016 NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_provenance.
- NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_assertion wasGeneratedBy ECO_0000203 NP924989.RASUBHfJ9r_LVT2bPQOG1yCVIfNo3Lr69d29k6tyrK9FY130_provenance.