Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_assertion description "[We found suggestive linkage of the BFNC phenotype to the 20q13-EBN1 locus (lod score, 2.03) and an intronic mutation IVS14-6 C>A in KCNQ2 segregating with the trait in all affected members, but absent in 100 unrelated control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_assertion evidence source_evidence_literature NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_assertion SIO_000772 16686649 NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_assertion wasDerivedFrom befree-20140225 NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_assertion wasGeneratedBy ECO_0000203 NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755844.RAodgWQ_8INoNJ0EWhHvj6oDwrykzeCXx6iwG7TgEH2KA130_provenance.