Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_assertion> ?p ?o ?g. }
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- NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_assertion type Assertion NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_head.
- NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_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." NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_provenance.
- NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_assertion evidence source_evidence_literature NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_provenance.
- NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_assertion SIO_000772 25728055 NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_provenance.
- NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_assertion wasDerivedFrom befree-2016 NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_provenance.
- NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_assertion wasGeneratedBy ECO_0000203 NP1267245.RAzXOM2ATIUdtE3t0E9w2NgkhkrmDHsgEaOBsV9F_mPYQ130_provenance.