Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP870985.RAkK6ixJAJroLXr71iE8A_ipq3ejhul3te0KtIEMebJ_E130_provenance.