Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_assertion wasGeneratedBy ECO_0000203 NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_assertion wasDerivedFrom befree-20140225 NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_assertion SIO_000772 17210889 NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_assertion evidence source_evidence_literature NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_assertion description "[The term `neuroacanthocytosis` is normally used to refer to autosomal recessive chorea-acanthocytosis and X-linked McLeod syndrome, but there are other movement disorders in which erythrocyte acanthocytosis may also be seen, such as Huntington disease-like 2 and pantothenate kinase-associated neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP828016.RAHlpg4QsuxhldsKJXFnoOatHM3R3gHJVMY3lzWIDEnEU130_provenance.