Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion> ?p ?o ?g. }
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- NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion type Assertion NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_head.
- NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion wasGeneratedBy ECO_0000203 NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_provenance.
- NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion wasDerivedFrom befree-20140225 NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_provenance.
- NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion SIO_000772 22236427 NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_provenance.
- NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion evidence source_evidence_literature NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_provenance.
- NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_assertion description "[The discovery that loss-of-function mutations in the gene DOCK8 are responsible for most forms of autosomal recessive hyper-IgE syndrome and some forms of combined immunodeficiency without elevated serum IgE has led to studies into the immunopathogenesis of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166445.RAHCuKOTw8RNpYOVKfTO6xwlBE1heG42nwCYjcI-83F8c130_provenance.