Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_assertion description "[Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_assertion evidence source_evidence_literature NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_assertion SIO_000772 24459211 NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_assertion wasDerivedFrom befree-20150227 NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_assertion wasGeneratedBy ECO_0000203 NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP356990.RAsM3_F89IrV0Mmdh35djtZUQ1jKV00nu2DCmtyNUA4lM130_provenance.