Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_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." NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_assertion evidence source_evidence_literature NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_assertion SIO_000772 16899997 NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_assertion wasDerivedFrom befree-2016 NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_assertion wasGeneratedBy ECO_0000203 NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.
- befree-2016 importedOn "2016-02-19" NP563628.RAf3VCNlZcCp2o25O8_3wfpkQbnn7ac-H3Cvudi3f3Vhg130_provenance.