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- source_evidence_literature type ECO_0000212 NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion description "[In four families, where the translocation co-segregated with the phenotype, one of the breakpoints concurred (at the cytogenetic level) with either a known dyslexia linkage region--at 15q21 (DYX1), 2p13 (DYX3) and 1p36 (DYX8)--or an unpublished linkage region at 19q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion evidence source_evidence_literature NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion SIO_000772 20798984 NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion wasDerivedFrom befree-20150227 NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion wasGeneratedBy ECO_0000203 NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_provenance.