Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_assertion description "[Cornelia de Lange syndrome (CdLS) is a dominantly inherited congenital malformation disorder, caused by mutations in the cohesin-loading protein NIPBL for nearly 60% of individuals with classical CdLS, and by mutations in the core cohesin components SMC1A (~5%) and SMC3 (<1%) for a smaller fraction of probands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_assertion evidence source_evidence_literature NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_assertion SIO_000772 22885700 NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_assertion wasDerivedFrom befree-20140225 NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_assertion wasGeneratedBy ECO_0000203 NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP670976.RA032n_d5tc61Mh7ncw8IHUhKYRr-pXDWdf-CnjXFUA5o130_provenance.