Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_assertion description "[genetic variants investigated in this study may be associated with a moderate modification of the risk for AD in some samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_assertion evidence source_evidence_literature NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_assertion SIO_000772 17387528 NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_assertion wasDerivedFrom gad-20150221 NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_assertion wasGeneratedBy ECO_0000203 NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82407.RAdvkbxSlB2UTOcO2rC1ygouR1zN1KUcpRrunVse3PICQ130_provenance.