Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_assertion wasGeneratedBy ECO_0000203 NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_assertion wasDerivedFrom befree-20140225 NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_assertion SIO_000772 16470731 NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_assertion evidence source_evidence_literature NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_assertion description "[Both phenotypes have been mapped to chromosome 18q21.1 and mutations in the DYM (dymeclin) gene were identified in 13 families with DMC and in two families with SMC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP704359.RA-yAbbObs3V67rslcUEekHSB_cwCRrwKi_iVVGU27ayg130_provenance.