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- NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_assertion type Assertion NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_head.
- NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_assertion description "[Deletion of the human SHANK3 gene near the terminus of chromosome 22q is associated with Phelan-McDermid syndrome and autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_assertion evidence source_evidence_literature NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_assertion SIO_000772 21048139 NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_assertion wasDerivedFrom befree-20140225 NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_assertion wasGeneratedBy ECO_0000203 NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.