Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_assertion description "[At present, eight different genes causing ADCAs have been found: spinocerebeller ataxia type 1 (SCA1), SCA2, SCA3/Machado-Joseph disease (MJD), SCA6, SCA7, SCA8, SCA12 and dentatorubropallidoluysian atrophy (DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_assertion evidence source_evidence_literature NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_assertion SIO_000772 11018707 NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_assertion wasDerivedFrom befree-20150227 NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_assertion wasGeneratedBy ECO_0000203 NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682023.RAVfPrJLjJPncbXJ7Z1YtML4ULDQpnCTLQrV3tAPKZXdQ130_provenance.