Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_assertion description "[Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune insulin-requiring diabetes associated with skeletal dysplasia and growth retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_assertion evidence source_evidence_literature NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_assertion SIO_000772 21050479 NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_assertion wasDerivedFrom befree-2016 NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_assertion wasGeneratedBy ECO_0000203 NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.
- befree-2016 importedOn "2016-02-19" NP850476.RANFX_KHGwMnVK72qYrCvX4yUewQAi8ZUq_-BOf8DD1Y8130_provenance.