Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_assertion description "[A de novo 7p21.1 deletion of 500 kb included the TWIST1 gene, a suggested candidate for RSTS that is responsible for the Saethre-Chotzen syndrome, an entity that enters in differential diagnosis with RSTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_assertion evidence source_evidence_literature NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_assertion SIO_000772 20125191 NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_assertion wasDerivedFrom befree-20140225 NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_assertion wasGeneratedBy ECO_0000203 NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP342047.RAVQ3MEmigH9_udxAH7t1Dm6dDtmXtVDuv4cWTaW3pEn8130_provenance.