Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_assertion> ?p ?o ?g. }
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- NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_assertion type Assertion NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_head.
- NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_assertion wasGeneratedBy ECO_0000203 NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_provenance.
- NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_assertion wasDerivedFrom befree-2016 NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_provenance.
- NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_assertion SIO_000772 17210889 NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_provenance.
- NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_assertion evidence source_evidence_literature NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_provenance.
- NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_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." NP587825.RAZyyG-n_McJnKy1dQLA-PFk1wLw9h9jUdhKUaaGwh1mg130_provenance.