Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_assertion description "[Dentatorubral-pallidoluysian atrophy (DRPLA) is a dominant hereditary neurodegenerative disorder caused by the expansion of a poly-glutamine (poly-Q) repeat in Atrophin-1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_assertion evidence source_evidence_literature NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_assertion SIO_000772 19681162 NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_assertion wasDerivedFrom befree-2016 NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_assertion wasGeneratedBy ECO_0000203 NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.
- befree-2016 importedOn "2016-02-19" NP757673.RAIIzB1fGcZaCZ-rVyGgCDB0BCWA9v89qkXHSMD4KT-ek130_provenance.