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- source_evidence_literature type ECO_0000212 NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_assertion description "[Aberrant methylation of the 11p15.5 imprinted region, through genetic or epigenetic mechanisms, leads to two clinical syndromes, with opposite growth phenotypes: Russell-Silver Syndrome (RSS; with severe fetal and postnatal growth retardation) and Beckwith-Wiedemann Syndrome (BWS; an overgrowth syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_assertion evidence source_evidence_literature NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_assertion SIO_000772 24322424 NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_assertion wasDerivedFrom befree-2016 NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_assertion wasGeneratedBy ECO_0000203 NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.
- befree-2016 importedOn "2016-02-19" NP1135239.RA1wsUlYXLEs5-32bDrFX-kwzAoF5iCMIu_KSGXBj_V18130_provenance.