Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_assertion description "[Chorea-acanthocytosis (ChAc; OMIM 200150) is a rare autosomal recessive disease with dysfunction of the erythrocyte membrane, presenting with acanthocytes and neurological manifestations characterized by progressive hyperkinesias (chorea, dystonia) and neuropsychological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_assertion evidence source_evidence_literature NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_assertion SIO_000772 16874760 NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_assertion wasDerivedFrom befree-20140225 NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_assertion wasGeneratedBy ECO_0000203 NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP277692.RAhDPsN6i5g4RpAp4XMjrzSuehDJ5ew4kKa-l_5XlmVdQ130_provenance.