Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion> ?p ?o ?g. }
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- NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion type Assertion NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_head.
- NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion description "[On analyzing CNTNAP2 polymorphisms in children with typical specific language impairment, we detected significant quantitative associations with nonsense-word repetition, a heritable behavioral marker of this disorder (peak association, P=5.0x10(-5) at SNP rs17236239).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_provenance.
- NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion evidence source_evidence_literature NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_provenance.
- NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion SIO_000772 18987363 NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_provenance.
- NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion wasDerivedFrom befree-20150227 NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_provenance.
- NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_assertion wasGeneratedBy ECO_0000203 NP881328.RAgnYBDU9j5SL_9k_XB424QFtoV5XAt3XXGFOOk0sxe1Y130_provenance.