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- source_evidence_literature type ECO_0000212 NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_assertion description "[These findings confirm that genetic variability in HTR(2A) contributes a small but significant degree of risk for the expression of TD, particularly in older patients and specifically for the non-orofacial (limb-truncal) type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_assertion evidence source_evidence_literature NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_assertion SIO_000772 15857569 NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_assertion wasDerivedFrom befree-20150227 NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_assertion wasGeneratedBy ECO_0000203 NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP390235.RANzMcnY88W5NYVb2HZZCo2H9Lhq_9t67xi38BQtEaQbo130_provenance.