Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion> ?p ?o ?g. }
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- NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion type Assertion NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_head.
- NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion description "[The Wiskott-Aldrich syndrome (WAS) is a primary immunodeficiency disease caused by mutations in the Wiskott-Aldrich Protein (WASP) gene, which typically leads to absent WASP protein expression in WAS leukocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_provenance.
- NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion evidence source_evidence_literature NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_provenance.
- NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion SIO_000772 17690954 NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_provenance.
- NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion wasDerivedFrom befree-20140225 NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_provenance.
- NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_assertion wasGeneratedBy ECO_0000203 NP447921.RAczoB0ns0gYVgQoUiGlhzTdCymCj0bJ4AiIAuAuzmQwY130_provenance.