Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_assertion description "[We delineated three regions that may contribute to the phenotype: a proximal one (chr1:164,501,003-167,022,133), associated with cardiac and renal anomalies, a distal one (chr1:178,514,910-181,269,712) and an intermediate 490 kb region (chr1:171970575-172460683, hg19), deleted in the most of the patients, and containing DNM3, MIR3120 and MIR214 that may play an important role in the phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_assertion evidence source_evidence_literature NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_assertion SIO_000772 25728055 NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_assertion wasDerivedFrom befree-2016 NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_assertion wasGeneratedBy ECO_0000203 NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267247.RAhLsS6V_gTy1JVD4M8fUHZDENwGsJTiyklVONNxlqZ44130_provenance.