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- NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_assertion type Assertion NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_head.
- NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_assertion wasGeneratedBy ECO_0000203 NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_provenance.
- NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_assertion wasDerivedFrom befree-2016 NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_provenance.
- NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_assertion SIO_000772 23350639 NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_provenance.
- NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_assertion evidence source_evidence_literature NP1047165.RAoAtZMoS3FXm-bMFRecLQJK6HUr8TjM0ZCMxhbUsT_e8130_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.