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- source_evidence_literature type ECO_0000212 NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP207595.RAZeo3XMcTJ40KspXa1f69QCdLInnCcFDIehFJ-FI2Nqo130_provenance.