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- source_evidence_literature type ECO_0000212 NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_assertion wasGeneratedBy ECO_0000203 NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_assertion wasDerivedFrom lhgdn-20090331 NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_assertion SIO_000772 16550584 NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_assertion evidence source_evidence_literature NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.