Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion description "[Mutations in the genes encoding the interacting proteins AML1 and CBFbeta are the most common genetic abnormalities in acute leukaemia, and congenital mutations in the related AML3 gene are associated with disorders of osteogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion evidence source_evidence_literature NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion SIO_000772 10856244 NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion wasDerivedFrom befree-20140225 NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion wasGeneratedBy ECO_0000203 NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance.