Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_assertion description "[MLL2, EP300, CREBBP, ASXL1) are also mutated in human developmental disorders thus pointing towards a remarkable and unexpected convergence between somatic and germline genetics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_assertion evidence source_evidence_literature NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_assertion SIO_000772 22287508 NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_assertion wasDerivedFrom befree-2016 NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_assertion wasGeneratedBy ECO_0000203 NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.
- befree-2016 importedOn "2016-02-19" NP956883.RAd37N80H3NCPEx2jyK_JByt9bWND_Q_KgQ2u3KnpwT1M130_provenance.