Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_assertion evidence source_evidence_literature NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_assertion SIO_000772 17673232 NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_assertion wasDerivedFrom befree-2016 NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_assertion wasGeneratedBy ECO_0000203 NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.