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- source_evidence_literature type ECO_0000212 NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_assertion description "[Tangier disease is a rare familial disorder characterized by enlarged orange tonsils, transient peripheral neuropathy, hepatosplenomegaly, and lymphadenopathy, as well as striking reductions in plasma high density lipoproteins (HDL) and their major protein constituents, apolipoproteins (apo)A-I and A-II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_assertion evidence source_evidence_literature NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_assertion SIO_000772 7130397 NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_assertion wasDerivedFrom befree-20140225 NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_assertion wasGeneratedBy ECO_0000203 NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP533591.RAN3IYFZU6zXWaGjId4Jxg5ip3P_2NP2_B1nH38EWuqCQ130_provenance.