Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_assertion description "[A novel 8.5 MB dup(1)(p34.1p34.3) characterized by FISH in a child presenting with congenital heart defect and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_assertion evidence source_evidence_literature NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_assertion SIO_000772 16892326 NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_assertion wasDerivedFrom befree-20140225 NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_assertion wasGeneratedBy ECO_0000203 NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870642.RA2TQJzGBPmoqT7SiTPOSCpXUk3gbHDWotqYImPewOgnM130_provenance.