Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_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." NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_assertion evidence source_evidence_literature NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_assertion SIO_000772 21050479 NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_assertion wasDerivedFrom befree-20150227 NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_assertion wasGeneratedBy ECO_0000203 NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1008102.RAVtpnoaG1Zb6mQkyza_yZsSB1XU3AVwNjn3f8xN1k-LM130_provenance.