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- source_evidence_literature type ECO_0000212 NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_assertion description "[DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_assertion evidence source_evidence_literature NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_assertion SIO_000772 2896160 NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_assertion wasDerivedFrom befree-20140225 NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_assertion wasGeneratedBy ECO_0000203 NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP579477.RASqe2-9e3j9EKJOxvw-IwItAGP3tN2-un6lbJ6hrE0dI130_provenance.