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- source_evidence_literature type ECO_0000212 NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_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." NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_assertion evidence source_evidence_literature NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_assertion SIO_000772 19656775 NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_assertion wasDerivedFrom befree-20150227 NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_assertion wasGeneratedBy ECO_0000203 NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP956569.RAvKxaBOxrHu8_sCN2aHfJdxGEGIgU_-biI4PHJ2eJCYw130_provenance.