Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_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." NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_assertion evidence source_evidence_literature NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_assertion SIO_000772 16874760 NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_assertion wasDerivedFrom befree-20150227 NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_assertion wasGeneratedBy ECO_0000203 NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP870168.RAses1ldHfjigaDE8-0XVFJbPwgLq0WU3wbnelhOCoJvU130_provenance.