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- source_evidence_literature type ECO_0000212 NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_assertion description "[We identified the missense mutation M520R in the calmodulin binding domain of the Kv7.1 channel from a German family with long QT-syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_assertion evidence source_evidence_literature NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_assertion SIO_000772 17482572 NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_assertion wasDerivedFrom befree-20150227 NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_assertion wasGeneratedBy ECO_0000203 NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP279093.RATxtBgChGikS2T_nk5Mckm0hKxEmb54XOIqZllxrcUcM130_provenance.