Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP719339.RAQLCLkEu2N2WdUd6WGM35SgKyRJSp5rPdaIqoMmd36xk130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719339.RAQLCLkEu2N2WdUd6WGM35SgKyRJSp5rPdaIqoMmd36xk130_provenance.
• NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719397.RAdC-JdqL9vrFzJFrw0wcwYJ8ey9N4HG7b-biSkyXmFUU130_provenance.
• NP978130.RAfYqASlj4WQ90xAWFUWJJwHezkA9lE7WCCk4vfl0AmJ4130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978130.RAfYqASlj4WQ90xAWFUWJJwHezkA9lE7WCCk4vfl0AmJ4130_provenance.
• NP978203.RAdskadCwiRtWdnhAGCjza38yynnxzwOcCqnGRveZ49iY130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978203.RAdskadCwiRtWdnhAGCjza38yynnxzwOcCqnGRveZ49iY130_provenance.
• assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP835558.RACyeE3P_HRuf6l322YJ-WOrLaExlgmTQjCoBi80JOZfQ130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835558.RACyeE3P_HRuf6l322YJ-WOrLaExlgmTQjCoBi80JOZfQ130_provenance.
• assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1128213.RAaO9eKjSUFTVX_J8JEuI-vL9RPg61ZX2LseETKKPkDbE130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128213.RAaO9eKjSUFTVX_J8JEuI-vL9RPg61ZX2LseETKKPkDbE130_provenance.
• NP1128216.RAUbdti43yt08I8lJ1kU_nETZnum9mPlZRaoV701HriT4130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128216.RAUbdti43yt08I8lJ1kU_nETZnum9mPlZRaoV701HriT4130_provenance.
• NP1128214.RAvxRT4dh07IPvMPpITI8L7bMRUKhEUr9xC1zsGemIT_c130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128214.RAvxRT4dh07IPvMPpITI8L7bMRUKhEUr9xC1zsGemIT_c130_provenance.
• NP1128218.RAqdMXsG_2-4iExHGXwr7SA4R47YoZjb49HQsKNfAsvtA130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128218.RAqdMXsG_2-4iExHGXwr7SA4R47YoZjb49HQsKNfAsvtA130_provenance.
• NP835505.RAOzcwuRqWvXQkNcZm2XRxfg6k-3dsNeaJ4apMLIwX4GY130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835505.RAOzcwuRqWvXQkNcZm2XRxfg6k-3dsNeaJ4apMLIwX4GY130_provenance.
• NP1128217.RANgYvjqClVZ51GSgx09tOYkwtvlsANTiSwTl8VUlCiBw130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128217.RANgYvjqClVZ51GSgx09tOYkwtvlsANTiSwTl8VUlCiBw130_provenance.
• NP1128215.RAwjMFStcUXp1Ak79LjR-y5R_5EqiR5o15O2xZ1wMbZIQ130_assertion description "[Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associated with abnormal genitalia), the most common mutation is the expansion of the first polyalanine tract of ARX, which results primarily in the clinical syndrome ISSX (infantile spasms).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128215.RAwjMFStcUXp1Ak79LjR-y5R_5EqiR5o15O2xZ1wMbZIQ130_provenance.