Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion> ?p ?o ?g. }
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- NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion type Assertion NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_head.
- NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion description "[Multiple system atrophy (MSA) is a rare neurodegenerative disease of undetermined cause manifesting with progressive autonomic failure (AF), cerebellar ataxia and parkinsonism due to neuronal loss in multiple brain areas associated with (oligodendro)glial cytoplasmic alpha-synuclein (alpha SYN) inclusions (GCIs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion evidence source_evidence_literature NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion SIO_000772 20493840 NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion wasDerivedFrom befree-20150227 NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_assertion wasGeneratedBy ECO_0000203 NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.