Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_assertion> ?p ?o ?g. }
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- NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_assertion type Assertion NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_head.
- NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_assertion wasGeneratedBy ECO_0000203 NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_provenance.
- NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_assertion wasDerivedFrom befree-20140225 NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_provenance.
- NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_assertion SIO_000772 17210889 NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_provenance.
- NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_assertion evidence source_evidence_literature NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_provenance.
- NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_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." NP158079.RA3q090Hh0Zvnp7hX6D61t9UIv9C4wRDb2DhRqwVz13IE130_provenance.