Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion> ?p ?o ?g. }
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- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion type Assertion NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_head.
- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_provenance.
- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion evidence source_evidence_literature NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_provenance.
- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion SIO_000772 22660720 NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_provenance.
- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion wasDerivedFrom befree-20140225 NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_provenance.
- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion wasGeneratedBy ECO_0000203 NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_provenance.