Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_assertion description "[MLL2 mutation carriers significantly more often presented with short stature and renal anomalies (p�=�0.026 and 0.031, respectively), and in addition, MLL2 carriers obviously showed more frequently a typical facial gestalt (17/19) compared with non-carriers (9/15), although this result was not statistically significant (p�=�0.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_assertion evidence source_evidence_literature NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_assertion SIO_000772 21607748 NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_assertion wasDerivedFrom befree-20140225 NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_assertion wasGeneratedBy ECO_0000203 NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615573.RA9DwnrspOKjdlVfKL0py5TbpAp4yswr-Z1PbaLdNla2k130_provenance.