Matches in Nanopublications for { ?s ?p "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP499909.RAD7Ze7aaY2fJJM2lKGdHQQiEKbjlk_ePRdqR9PIS7Yvo130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499909.RAD7Ze7aaY2fJJM2lKGdHQQiEKbjlk_ePRdqR9PIS7Yvo130_provenance.
- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499910.RAcCVqWC1b5p99lLPphdbp9QJ80BU5DT22cF1iof14cm4130_provenance.
- NP499907.RAGZYVRX46KUpwkEvS7cZ9ssvx5GW9A0b86BHAjjeOQ5M130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499907.RAGZYVRX46KUpwkEvS7cZ9ssvx5GW9A0b86BHAjjeOQ5M130_provenance.