Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion> ?p ?o ?g. }
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- NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion type Assertion NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_head.
- NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion description "[Here we have addressed the allelic diversity of the DISC1, DISC2 and TRAX genes, clustered in 1q42, in Finnish families ascertained for infantile autism (97 families, n(affected)=138) and Asperger syndrome (29 families, n(affected)=143).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_provenance.
- NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion evidence source_evidence_literature NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_provenance.
- NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion SIO_000772 17579608 NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_provenance.
- NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion wasDerivedFrom befree-2016 NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_provenance.
- NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_assertion wasGeneratedBy ECO_0000203 NP616026.RA1nicVF9QgiBEw3KIZWqcCdikL5_75pEILqUbnJ_92_s130_provenance.