Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_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." NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion evidence source_evidence_literature NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion SIO_000772 17673232 NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion wasDerivedFrom befree-20140225 NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion wasGeneratedBy ECO_0000203 NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.