Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_assertion description "[We identified the p.G2019S in one AD patient with no PD signs, indicating that this mutation is not a common etiological factor for AD in our population (0.5%), corroborating recent data found in Norwegian, North American, Chinese and Italian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_assertion evidence source_evidence_literature NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_assertion SIO_000772 19822953 NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_assertion wasDerivedFrom befree-20140225 NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_assertion wasGeneratedBy ECO_0000203 NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP393005.RA4ndTWw7lvXW5lDMO9iXkiv1xKfeplkhqxq0OenZxT1U130_provenance.