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- source_evidence_literature type ECO_0000212 NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_assertion description "[In some such families, desmin or alpha-B crystallin gene mutation is the underlying cause, and the desmin accumulation affects skeletal muscle as well, usually causing skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_assertion evidence source_evidence_literature NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_assertion SIO_000772 11298680 NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_assertion wasDerivedFrom befree-20150227 NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_assertion wasGeneratedBy ECO_0000203 NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP328335.RAhxriIi2338cH6PMxlE0v7JepgTN2SYi1brDMYlE36uw130_provenance.