Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_assertion description "[We identified three genetic variants (haplotypes) of the gene encoding catecholamine-O-methyltransferase (COMT) that we designated as low pain sensitivity (LPS), average pain sensitivity (APS) and high pain sensitivity (HPS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_assertion evidence source_evidence_literature NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_assertion SIO_000772 15537663 NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_assertion wasDerivedFrom befree-20140225 NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_assertion wasGeneratedBy ECO_0000203 NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP482220.RAJeSjzh1AxCX3HN9rIcM4gH01vpe-3hgwDA3SnCU3hDE130_provenance.