Matches in Nanopublications for { ?s ?p "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion description "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_assertion description "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880422.RAz_enj45rHskKichpthZJJvqD0M4WxpuLxqTA5JQd8-4130_provenance.
- NP950800.RA2L4oFaHZmaJGwzWwDQQSwJGk-XFgRN8wedpaoxC13Rg130_assertion description "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950800.RA2L4oFaHZmaJGwzWwDQQSwJGk-XFgRN8wedpaoxC13Rg130_provenance.
- NP332579.RAlvuuWd065UA2k3weiXmfp9DG69ZGwEZr-E8hFs7sOTs130_assertion description "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332579.RAlvuuWd065UA2k3weiXmfp9DG69ZGwEZr-E8hFs7sOTs130_provenance.
- NP950801.RAj-9mEh9VafdWazd0woFrv_uAqJ9loULMrieNRcbqvz8130_assertion description "[There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950801.RAj-9mEh9VafdWazd0woFrv_uAqJ9loULMrieNRcbqvz8130_provenance.