Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_assertion description "[The findings support the association of several loci with AD, and suggest how intermediate phenotypes can enhance analysis of susceptibility loci in this complex genetic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_assertion evidence source_evidence_literature NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_assertion SIO_000772 20574532 NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_assertion wasDerivedFrom gad-20130706 NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_assertion wasGeneratedBy ECO_0000203 NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP70258.RAl6hO1T_0WWBaxn5vV2NEAFHAFV69-tPqTxQP9q6HtgA130_provenance.