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- source_evidence_literature type ECO_0000212 NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_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." NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_assertion evidence source_evidence_literature NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_assertion SIO_000772 19656775 NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_assertion wasDerivedFrom befree-2016 NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_assertion wasGeneratedBy ECO_0000203 NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP755571.RAUJ2Ajf_SM3ZJvCOvAp9X1b3jxjn51TPcy1V2iCb8aQ4130_provenance.