Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion type Assertion NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_head.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion description "[Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_provenance.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion evidence source_evidence_literature NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_provenance.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion SIO_000772 15892853 NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_provenance.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion wasDerivedFrom befree-2016 NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_provenance.
- NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_assertion wasGeneratedBy ECO_0000203 NP494669.RAkutb-TDYXQ5aNxLBMIZSIQTVeNbXE59ubskJU_nVOTs130_provenance.