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- source_evidence_literature type ECO_0000212 NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_assertion description "[The incidence of PMD with PLP1 mutations was estimated to be 1.45 per 100,000 male live births and that for congenital hypomyelinating disorders with unknown cause to be 0.41 per 100,000 live births.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_assertion evidence source_evidence_literature NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_assertion SIO_000772 24532200 NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_assertion wasDerivedFrom befree-20150227 NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_assertion wasGeneratedBy ECO_0000203 NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP631456.RAVHK09ItM97Au-SRUfsuvawHOmgF-3yLlU597hwO8rbk130_provenance.