Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion> ?p ?o ?g. }
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- NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion type Assertion NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_head.
- NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion description "[AOA1 is associated with oculomotor apraxia, severe sensorimotor neuropathy, choreiform movements, cognitive impairment, and cerebellar atrophy at an early age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_provenance.
- NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion evidence source_evidence_literature NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_provenance.
- NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion SIO_000772 16700949 NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_provenance.
- NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion wasDerivedFrom befree-20150227 NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_provenance.
- NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_assertion wasGeneratedBy ECO_0000203 NP914839.RAnplJvAnlIx7L7SSegZuMm5Uz9vyMd9hK6gwtwzzvkYE130_provenance.