Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_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." NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_assertion evidence source_evidence_literature NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_assertion SIO_000772 21934608 NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_assertion wasDerivedFrom befree-2016 NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_assertion wasGeneratedBy ECO_0000203 NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP925245.RAohUs7rIOYvr4jAzXXRE2h52J709wXJGuNnIqfxXsMlQ130_provenance.