Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_assertion description "[We describe a 5-month-old boy with complex congenital heart defects (dTGA, DORV, VSD, ASD, and PDA), minor facial and ear anomalies, deep palmar creases, multiple vertebral anomalies, agenesis of the corpus callosum, and mosaic tetrasomy 8p (47,XY,+i(8)(p10)[88%]/46,XY[12%] in blood with normal chromosomes in cultured skin fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_assertion evidence source_evidence_literature NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_assertion SIO_000772 9415694 NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_assertion wasDerivedFrom befree-20140225 NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_assertion wasGeneratedBy ECO_0000203 NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP530070.RAnJHNZDeJzKDyzLSCgsQbOI10MhGcWT_fgsWItPj-RNA130_provenance.