Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_assertion description "[Given the overlap of this autism/mental retardation (MR) phenotype and the MR-associated disorders in our patients, together with the fact that mapping of the additional autosomal breakpoints involved did not disclose obvious candidate disease genes, we ascertain with this study that AUTS2 mutations are clearly linked to autosomal dominant mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_assertion evidence source_evidence_literature NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_assertion SIO_000772 17211639 NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_assertion wasDerivedFrom befree-20140225 NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_assertion wasGeneratedBy ECO_0000203 NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746409.RADtSwvBHOaLKqUpWFlzgoXSNgVD2s7SQc3q1vqT9axzs130_provenance.