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- source_evidence_literature type ECO_0000212 NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_assertion description "[Within two of these loci, DYX1C1 (15q21) and ROBO1 (3p12) have recently been proposed as dyslexia candidate genes through the molecular analysis of translocation breakpoints in dyslexic individuals carrying balanced chromosomal translocations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_assertion evidence source_evidence_literature NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_assertion SIO_000772 18521840 NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_assertion wasDerivedFrom befree-20140225 NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_assertion wasGeneratedBy ECO_0000203 NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP762950.RAGRmo_11cqnjyY7EZ0Y3_WwQdBZjEaDrjkCmruOJ1_fw130_provenance.