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- source_evidence_literature type ECO_0000212 NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_assertion wasGeneratedBy ECO_0000203 NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_assertion wasDerivedFrom befree-20140225 NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_assertion SIO_000772 19648161 NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_assertion evidence source_evidence_literature NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_assertion description "[The low mutation frequency and the absence of biallelic destructive mutations propose a minor contribution of NFKBIA and TNFAIP3 mutations to the NF-kappaB activity of NLPHL, suggesting different mechanisms of NF-kappaB activation in NLPHL and cHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP866591.RAE8_vdR2-313AEw_PWa0EU3Z7LcOngz1XaS8G-0QdEH8130_provenance.