Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion> ?p ?o ?g. }
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- NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion type Assertion NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_head.
- NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion description "[Paternal uniparental disomy 14 (UPD(14)pat) results in a unique constellation of clinical features, and a similar phenotypic constellation is also caused by microdeletions involving the DLK1-MEG3 intergenic differentially methylated region (IG-DMR) and/or the MEG3-DMR and by epimutations (hypermethylations) affecting the DMRs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_provenance.
- NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion evidence source_evidence_literature NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_provenance.
- NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion SIO_000772 22353941 NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_provenance.
- NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion wasDerivedFrom befree-20150227 NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_provenance.
- NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_assertion wasGeneratedBy ECO_0000203 NP961042.RAsb91nQmVYiet0p_rviDUO2xsokjvdL5dTPnh_Uudj4w130_provenance.