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- source_evidence_literature type ECO_0000212 NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_assertion description "[Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_assertion evidence source_evidence_literature NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_assertion SIO_000772 19086034 NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_assertion wasDerivedFrom befree-20150227 NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_assertion wasGeneratedBy ECO_0000203 NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP944606.RAYUTTQTB4nR4eHynoyFbo_WHGaLdPvWM2S60C1QuTHYA130_provenance.