Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_assertion type Assertion NP465152.RAYvvgldfDK2VN95NtOAL_RD9fP9tbyA5dKRwURQyUOrU130_head.
- 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.