Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion type Assertion NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_head.
- NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion description "[Emery-Dreifuss muscular dystrophy (EDMD1) is caused by mutations in either the X-linked gene emerin (EMD) or the autosomal lamin A/C (LMNA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_provenance.
- NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion evidence source_evidence_literature NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_provenance.
- NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion SIO_000772 16403804 NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_provenance.
- NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion wasDerivedFrom befree-20140225 NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_provenance.
- NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_assertion wasGeneratedBy ECO_0000203 NP939375.RAsrj3rDHdiFN5knO9P--7ZA7RlK9GWibMvZwFGSrHqSU130_provenance.