Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_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." NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_assertion evidence source_evidence_literature NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_assertion SIO_000772 19681162 NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_assertion wasDerivedFrom befree-20150227 NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_assertion wasGeneratedBy ECO_0000203 NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP361250.RAaW33cRNLIRSKWBIBhKjSSR7IkTpJN2ZoFrO4sM4_2HY130_provenance.