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- NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_assertion type Assertion NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_head.
- NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_assertion wasGeneratedBy ECO_0000203 NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_provenance.
- NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_assertion wasDerivedFrom befree-20150227 NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_provenance.
- NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_assertion SIO_000772 16615080 NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_provenance.
- NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_assertion evidence source_evidence_literature NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_provenance.
- NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_assertion description "[Interestingly, a similar epigenetic alteration (with loss of methylation) at a putative ICR on human chromosome 6q24, is involved in transient neonatal diabetes mellitus (TNDM), a congenital disease with intrauterine growth retardation and a transient lack of insulin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512271.RA5qjtkTqIM1q_zd_-JN_U6fyXSi_-Aqent-rylAL7cPo130_provenance.