Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_assertion description "[The imprinted Snurf-Snrpn chromosomal domain contains two large arrays of tandemly repeated, paternally expressed box C/D small-nucleolar RNA (snoRNA) genes: the SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters believed to play key roles in the fine-tuning of serotonin receptor (5-HT2C) pre-mRNA processing and in the etiology of the Prader-Willi Syndrome (PWS), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_assertion evidence source_evidence_literature NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_assertion SIO_000772 22495932 NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_assertion wasDerivedFrom befree-20150227 NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_assertion wasGeneratedBy ECO_0000203 NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959252.RAwK2oCldIpiucnOLSdlSXmX8CBuZp4qb4NTJqmelqiwM130_provenance.