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- source_evidence_literature type ECO_0000212 NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_assertion evidence source_evidence_literature NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_assertion SIO_000772 18807109 NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_assertion wasDerivedFrom befree-20140225 NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_assertion wasGeneratedBy ECO_0000203 NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.
- befree-20140225 importedOn "2014-02-25" NP704743.RAj44CPn_gNpfQuINjkgCv5Ev5bIWe8LPHorkS_NgNx68130_provenance.