Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_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." NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_assertion evidence source_evidence_literature NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_assertion SIO_000772 16899997 NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_assertion wasDerivedFrom befree-20150227 NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_assertion wasGeneratedBy ECO_0000203 NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP331069.RA538dfsTjzcGkuCI25rUjyGZwToCPx6z2G3RC4ne1VGo130_provenance.