Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion> ?p ?o ?g. }
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- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion type Assertion NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_head.
- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance.
- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion evidence source_evidence_literature NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance.
- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion SIO_000772 17262171 NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance.
- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion wasDerivedFrom befree-20150227 NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance.
- NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_assertion wasGeneratedBy ECO_0000203 NP767214.RA_VSgtB0MtSYkJMC8ZTr7Lote3A7kFWiGoeKtrCDZwIs130_provenance.