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- NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_assertion type Assertion NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_head.
- 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.
- NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_assertion evidence source_evidence_literature NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_provenance.
- NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_assertion SIO_000772 15892853 NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_provenance.
- NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_assertion wasDerivedFrom befree-2016 NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_provenance.
- NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_assertion wasGeneratedBy ECO_0000203 NP494671.RAXfYfjcHE_KSHkrQANwfCjJg3rhy7B3aEls-wYKyp6ro130_provenance.