Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_assertion description "[These findings suggest that such protein CSF changes may help to support the clinical diagnosis of cognitive decline in PD and that there may be apolipoprotein-E-isoform-specific differences in CSF protein regulation in advanced PDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_assertion evidence source_evidence_literature NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_assertion SIO_000772 16899997 NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_assertion wasDerivedFrom befree-20140225 NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_assertion wasGeneratedBy ECO_0000203 NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868212.RAZd8qjerhqBRO4SXbntxaiNkcvYB_5CLggUWb12A1_iM130_provenance.