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- source_evidence_literature type ECO_0000212 NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_assertion description "[Dystonia musculorum (dt) is an autosomal recessive hereditary neuropathy with a characteristic uncoordinated movement and is caused by a defect in the bullous pemphigoid antigen 1 (BPAG1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_assertion evidence source_evidence_literature NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_assertion SIO_000772 21272373 NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_assertion wasDerivedFrom befree-20150227 NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_assertion wasGeneratedBy ECO_0000203 NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270251.RADzo9kTrTDKLPXlKQWmBgk2CV_OsC5tfkAdAOYN39ePo130_provenance.