Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP697052.RAFNkFXjsUQzPHObJ73tDQwGqdORD18aV89OhdxIYAGzI130_provenance.