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- source_evidence_literature type ECO_0000212 NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_assertion evidence source_evidence_literature NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_assertion SIO_000772 23759358 NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_assertion wasDerivedFrom befree-20150227 NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_assertion wasGeneratedBy ECO_0000203 NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.