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- source_evidence_literature type ECO_0000212 NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_assertion description "[Welander distal myopathy (WDM) is an autosomal dominant myopathy with late-adult onset characterized by slow progression of distal muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_assertion evidence source_evidence_literature NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_assertion SIO_000772 10482271 NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_assertion wasDerivedFrom befree-2016 NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_assertion wasGeneratedBy ECO_0000203 NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.
- befree-2016 importedOn "2016-02-19" NP262679.RAvp3sfkRp2Vv0M1x3bsoCM-67W_hI-685gh-1sySCVug130_provenance.