Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_assertion description "[Using 100 families having at least two siblings affected with dyslexia, model-free linkage analysis revealed evidence for linkage to the DRD4-exon 3 repeat (two-point MFLOD = 2.27, P = 0.001) and to HRAS located just proximal to DRD4 (two-point MFLOD = 2.68, P = 0.0004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_assertion evidence source_evidence_literature NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_assertion SIO_000772 14755455 NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_assertion wasDerivedFrom befree-2016 NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_assertion wasGeneratedBy ECO_0000203 NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.
- befree-2016 importedOn "2016-02-19" NP430230.RABUmqMWjr4COvtJFNgDzBD1k7e2vNroAHGiMYC_hlmQA130_provenance.