Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_assertion description "[The influence of GRN genetic variability on susceptibility to AD and on expression levels in a series of neuropathologically-confirmed AD patients as well as in peripheral mononuclear cells (PBMC) and in cells isolated from cerebrospinal fluid (CSF) was investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_assertion evidence source_evidence_literature NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_assertion SIO_000772 19625741 NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_assertion wasDerivedFrom befree-2016 NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_assertion wasGeneratedBy ECO_0000203 NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.
- befree-2016 importedOn "2016-02-19" NP752967.RAWE1JD3KsLmlvPIoxVj6YYE7RUiEVNguQdy39C3LVzzY130_provenance.