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- source_evidence_literature type ECO_0000212 NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_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." NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_assertion evidence source_evidence_literature NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_assertion SIO_000772 19656775 NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_assertion wasDerivedFrom befree-20150227 NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_assertion wasGeneratedBy ECO_0000203 NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959218.RAMpZg_5jmL3JwzayS9urDUiyw6bL5SstouqMR9AWt7Dg130_provenance.