Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959926.RADY52z5sdQlyKo3yuLXHPkqraJYkwR-znv1NdcTWDNdk130_provenance.
• NP314432.RAUsr3huXNzISoC2GGLYL_os5av-xLikMVzyTIMGRVb4s130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314432.RAUsr3huXNzISoC2GGLYL_os5av-xLikMVzyTIMGRVb4s130_provenance.
• assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP866227.RA3LmMtN1sjfsbBCou5ugzwg3T0LKcCKnWpj0WRZVZvOU130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866227.RA3LmMtN1sjfsbBCou5ugzwg3T0LKcCKnWpj0WRZVZvOU130_provenance.
• NP959901.RA_qVVXTIAAIknS-Qfxfx0Rq9mbOsAUt3jCOeZRCO59ZM130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959901.RA_qVVXTIAAIknS-Qfxfx0Rq9mbOsAUt3jCOeZRCO59ZM130_provenance.
• assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1047170.RA2FORHutOMv-P0PX2U5CFY7jOTrfV1ji44Jcpb1ozhd4130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1047170.RA2FORHutOMv-P0PX2U5CFY7jOTrfV1ji44Jcpb1ozhd4130_provenance.
• NP1047169.RAZf9NXPQRAoJ7BchJfA4UKg47jUfLMRR8hf-FGCmB0Vc130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1047169.RAZf9NXPQRAoJ7BchJfA4UKg47jUfLMRR8hf-FGCmB0Vc130_provenance.
• assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866236.RAPAAhyeTI8rsS5eoGY-IBfm-X_K1bAHqEIO9mDuLZBaw130_provenance.
• NP314458.RAnyUpUYMjO1wKyaLsG2XiHz6zo1m_d9VlMsew-Kmj1Ig130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314458.RAnyUpUYMjO1wKyaLsG2XiHz6zo1m_d9VlMsew-Kmj1Ig130_provenance.
• NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_assertion description "[Co-occurrence of a de novo SHANK2 mutation and a CHRNA7 duplication in two reported patients with ASD and ID as well as in the patient with t(11;17;19), severe ID and behavior problems suggests convergence of these genes on a common synaptic pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_provenance.