Matches in Nanopublications for { ?s ?p "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1116299.RAeGBLxBmIMQ6_9W6x3e_clfr-LIh0ynJ0sgc5xSPPdpw130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116299.RAeGBLxBmIMQ6_9W6x3e_clfr-LIh0ynJ0sgc5xSPPdpw130_provenance.
- NP1116301.RAft2XTTuOA8M0ZinhYY2e57eKeWjuDLyHXMt_TGBvIU0130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116301.RAft2XTTuOA8M0ZinhYY2e57eKeWjuDLyHXMt_TGBvIU0130_provenance.
- NP720026.RAknUYKuAGyOmwA3m0Z5qjg1n2ENbK3pFo6afw6DpClME130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720026.RAknUYKuAGyOmwA3m0Z5qjg1n2ENbK3pFo6afw6DpClME130_provenance.
- NP719986.RAC8F-2Mnf4hvffnSK2YiQXGMZ6iFVhdqzmbiN-RtP_1Q130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719986.RAC8F-2Mnf4hvffnSK2YiQXGMZ6iFVhdqzmbiN-RtP_1Q130_provenance.
- NP1116300.RAuSDH-z7AV0Jd1Kzpd3lBl-jT2u55bUgXFODvPpVvigY130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116300.RAuSDH-z7AV0Jd1Kzpd3lBl-jT2u55bUgXFODvPpVvigY130_provenance.
- NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_assertion description "[STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719992.RA3dVTJmAJ99u9Og4C30iJiy3yspT5gfqfyQ5M8toRDGc130_provenance.