Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_assertion description "[This clustering of novel mutations in the POT1 binding domain of ACD was statistically higher (P = .005) in melanoma probands compared with population control individuals (n = 6785), as were all novel and rare variants in both ACD (P = .040) and TERF2IP (P = .022).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_assertion evidence source_evidence_literature NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_assertion SIO_000772 25505254 NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_assertion wasDerivedFrom befree-2016 NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_assertion wasGeneratedBy ECO_0000203 NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248144.RAm_S7bQcwVSH2cRHA3jRpNnplykTYe60r79Tr0G6o9mA130_provenance.