Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_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." NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_assertion evidence source_evidence_literature NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_assertion SIO_000772 19656775 NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_assertion wasDerivedFrom befree-20150227 NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_assertion wasGeneratedBy ECO_0000203 NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959185.RAfZGM3T0DmeiiMGXbtoOaSczkoi0jFZlS3S-prZV0rN8130_provenance.