Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- befree-2016 importedOn "2016-02-19" NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_assertion wasGeneratedBy ECO_0000203 NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_assertion wasDerivedFrom befree-2016 NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_assertion SIO_000772 21607748 NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_assertion evidence source_evidence_literature NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.
- NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_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." NP896459.RA1_zB3xkgNFqLkMF3CvKIAjQ47OEhwbgPtUs3BXM_sWA130_provenance.