Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion> ?p ?o ?g. }
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- NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion type Assertion NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_head.
- NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion description "[These results indicate that mutations in NLGN3 and NLGN4 genes are responsible for at most a small fraction of autism cases and additional screenings in other autistic populations are needed to better determine the frequency with which mutations in NLGN3 and NLGN4 occur in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_provenance.
- NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion evidence source_evidence_literature NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_provenance.
- NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion SIO_000772 15389766 NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_provenance.
- NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion wasDerivedFrom befree-20140225 NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_provenance.
- NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_assertion wasGeneratedBy ECO_0000203 NP477401.RA5dyFsArAIEtzVDkCVfMkODlNlF8RK_6tAV78Xrn6Gi4130_provenance.