Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion> ?p ?o ?g. }
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- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion type Assertion NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_head.
- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion wasGeneratedBy ECO_0000203 NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_provenance.
- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion wasDerivedFrom befree-2016 NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_provenance.
- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion SIO_000772 20730472 NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_provenance.
- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion evidence source_evidence_literature NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_provenance.
- NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834379.RARhO5mcMHfIvH1uF2-cLLVJuQ32V8jwUpMuiuusFlDyc130_provenance.