Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_assertion evidence source_evidence_literature NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_assertion SIO_000772 9217978 NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_assertion wasDerivedFrom befree-20140225 NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_assertion wasGeneratedBy ECO_0000203 NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.
- befree-20140225 importedOn "2014-02-25" NP515617.RATDX2eDPNp2bqbB9hZGh3c7HvqYxGW5lGkQrPQc5Lu40130_provenance.