Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_assertion description "[Further analyses after birth, using C-banding, NOR staining and fluorescence in situ hybridization (FISH) with telomeric probes, revealed that it was the result of an unbalanced de novo t(11;14)(p15;p13) translocation leading to partial 11p trisomy and to BWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_assertion evidence source_evidence_literature NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_assertion SIO_000772 11241533 NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_assertion wasDerivedFrom befree-20140225 NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_assertion wasGeneratedBy ECO_0000203 NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860834.RAn_dkqCKhHsWZnsiHX5wwu-Ofw_zXeNZRQPV1BBYic_A130_provenance.