Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_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." NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_assertion evidence source_evidence_literature NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_assertion SIO_000772 17673232 NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_assertion wasDerivedFrom befree-20150227 NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_assertion wasGeneratedBy ECO_0000203 NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.