Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion> ?p ?o ?g. }
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- NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion type Assertion NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_head.
- NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion description "[The likelihood of a paternally expressing imprinted gene in chromosome region 6(q23-24) has been highlighted by cases of transient neonatal diabetes mellitus (TNDM) in which paternal uniparental disomy (UPD) for chromosome 6 or paternal duplication 6(q23-qter) was detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_provenance.
- NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion evidence source_evidence_literature NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_provenance.
- NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion SIO_000772 10323737 NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_provenance.
- NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion wasDerivedFrom befree-20140225 NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_provenance.
- NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_assertion wasGeneratedBy ECO_0000203 NP380931.RAKb-fBV-5RgQuNMmFiQeZ7XQkjMMvOeT1Aon51EGZDp0130_provenance.