Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_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." NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_assertion evidence source_evidence_literature NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_assertion SIO_000772 22287508 NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_assertion wasDerivedFrom befree-20140225 NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_assertion wasGeneratedBy ECO_0000203 NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768504.RAuP1WLPvNC4vewoiZ8Jf98MidIQv4ZXncXVf05Jjfxcg130_provenance.