Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion type Assertion NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_head.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion evidence source_evidence_literature NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion SIO_000772 15520409 NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion wasDerivedFrom lhgdn-20090331 NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_assertion wasGeneratedBy ECO_0000203 NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.