Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion> ?p ?o ?g. }
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- NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_assertion type Assertion NP992208.RAyBWA-7dPHJCQAKS1v0rnBuG79g7CXIzyKKhDysy--v0130_head.
- 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the cytogenetic level) with either a known dyslexia linkage region--at 15q21 (DYX1), 2p13 (DYX3) and 1p36 (DYX8)--or an unpublished linkage region at 19q13.].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.