Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion> ?p ?o ?g. }
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- NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion type Assertion NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_head.
- NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_provenance.
- NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion evidence source_evidence_literature NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_provenance.
- NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion SIO_000772 8737929 NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_provenance.
- NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion wasDerivedFrom befree-20150227 NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_provenance.
- NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion wasGeneratedBy ECO_0000203 NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_provenance.