Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion> ?p ?o ?g. }
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- NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion type Assertion NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_head.
- NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion description "[WHIM is an acronym for a rare immunodeficiency syndrome (OMIM #193670) caused by autosomal dominant mutations truncating the C-terminus of the chemokine receptor CXC chemokine receptor 4 (CXCR4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_provenance.
- NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion evidence source_evidence_literature NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_provenance.
- NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion SIO_000772 21070597 NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_provenance.
- NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion wasDerivedFrom befree-20140225 NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_provenance.
- NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_assertion wasGeneratedBy ECO_0000203 NP783883.RA6aAbK0eJhk_JJDHv9BdBTUj1fImhZoDItG6rk8kcTmQ130_provenance.