Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_assertion description "[Deficiency of the paternal 15q11-q13 snoRNA HBII-85 locus is necessary to cause the neurodevelopmental disorder Prader-Willi syndrome (PWS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_assertion evidence source_evidence_literature NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_assertion SIO_000772 19656775 NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_assertion wasDerivedFrom befree-20150227 NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_assertion wasGeneratedBy ECO_0000203 NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1005889.RAgtJxTo25-YzdOt_L1tw59GMJDQPOYs9JmcT6YtNJ1Ds130_provenance.