Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_assertion description "[Rare individuals with PWS who carry atypical microdeletions on chromosome 15q have narrowed the critical region for this disorder to a 108 kb region that includes the SNORD116 snoRNA cluster and the Imprinted in Prader-Willi (IPW) non-coding RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_assertion evidence source_evidence_literature NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_assertion SIO_000772 24363065 NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_assertion wasDerivedFrom befree-20150227 NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_assertion wasGeneratedBy ECO_0000203 NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP956552.RAJQmxegsTDu2E-SQ40eXH86XZKrtnXa1B7MADkCXLa1g130_provenance.