Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_assertion description "[Patients with BPES carrying larger deletions encompassing FOXL2 present more frequently with associated clinical findings, such as mental retardation (D?haene et al., 2009).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_assertion evidence source_evidence_literature NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_assertion SIO_000772 21934608 NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_assertion wasDerivedFrom befree-20140225 NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_assertion wasGeneratedBy ECO_0000203 NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP575250.RAAu2VsVnIcM_O5MXuvV2S2qG1jkMuu9bnYR-JqOVf_Xs130_provenance.