Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion> ?p ?o ?g. }
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- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion type Assertion NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_head.
- 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.