Matches in Nanopublications for { ?s ?p "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP465937.RAul85ivT2iVLhc9QD6Anw6y9ZeVvNt6X67tCLLmtWrV8130_assertion description "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465937.RAul85ivT2iVLhc9QD6Anw6y9ZeVvNt6X67tCLLmtWrV8130_provenance.
- assertion description "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_assertion description "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion description "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_provenance.