Matches in Nanopublications for { ?s ?p "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357952.RAlsbPFQeuDN9ag16nv1CRZ_qEVA21TkIjqJ-0Cw2X_iA130_provenance.
- NP912043.RAbcVjol8XdYWdEyxm2uH0Oi92X3umomVRXz1uUkSjAWI130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912043.RAbcVjol8XdYWdEyxm2uH0Oi92X3umomVRXz1uUkSjAWI130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21412.RAvGQWbSay5MkQO2pbOgIqqg_e-jJo07fqsLvrvt7KYaI130_provenance.
- NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114611.RA-fIWhd1-1X4Jfhtg_3JVuH-Owu-9U3UsBeVneXRe-RI130_provenance.
- NP1114613.RA_kbrVCrX7JtouZRVHlCxuXMHUDvMgQp4cUyhKmnLVKo130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114613.RA_kbrVCrX7JtouZRVHlCxuXMHUDvMgQp4cUyhKmnLVKo130_provenance.
- assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.