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- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion type Assertion NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_head.
- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion wasGeneratedBy ECO_0000203 NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_provenance.
- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion wasDerivedFrom befree-20150227 NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_provenance.
- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion SIO_000772 9684781 NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_provenance.
- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion evidence source_evidence_literature NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_provenance.
- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_provenance.