Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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." provenance.
- NP851929.RAAkRrjTDAr8RcYkjHxDZELyoF0mkSFGJHjeFxdREE7Ps130_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." NP851929.RAAkRrjTDAr8RcYkjHxDZELyoF0mkSFGJHjeFxdREE7Ps130_provenance.
- NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_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." NP784603.RAxLc5p7E0aAqyNZ3l2I_BIyB5n5gzqfmFRdzSueMwiGw130_provenance.