Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion> ?p ?o ?g. }
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- NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion type Assertion NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_head.
- NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion description "[It is now recognized that p53 activation, caused by haploinsufficiency for the ribosomal gene RPS14 (mapping to the commonly deleted region), is the probable cause of the erythroid defect in the 5q- syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_provenance.
- NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion evidence source_evidence_literature NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_provenance.
- NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion SIO_000772 22571696 NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_provenance.
- NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion wasDerivedFrom befree-20150227 NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_provenance.
- NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_assertion wasGeneratedBy ECO_0000203 NP675886.RAcMxeNn2X79q5QaP0Zg2eUcLXjgTsIvvTK_Tjs5Cx3iQ130_provenance.