Matches in Nanopublications for { ?s ?p "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_provenance.
- NP389420.RAE2sMlP3GK1kctahUCdiF7VLFRr043kSLjwQlhlAVxH4130_assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389420.RAE2sMlP3GK1kctahUCdiF7VLFRr043kSLjwQlhlAVxH4130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP494670.RAyEWEcoOFnTwJVXpA62k_o3ETUGWbnqjDLZfHAL34t5s130_assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494670.RAyEWEcoOFnTwJVXpA62k_o3ETUGWbnqjDLZfHAL34t5s130_provenance.