Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_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." NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_assertion evidence source_evidence_literature NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_assertion SIO_000772 14755455 NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_assertion wasDerivedFrom befree-20150227 NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_assertion wasGeneratedBy ECO_0000203 NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_provenance.