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- source_evidence_literature type ECO_0000212 NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_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." NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_assertion evidence source_evidence_literature NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_assertion SIO_000772 21050479 NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_assertion wasDerivedFrom befree-20150227 NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_assertion wasGeneratedBy ECO_0000203 NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP512417.RA2-aMi-AQqIr0PufpmX7CLVuM4hIQNJMmdhndlYZguu8130_provenance.