Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion> ?p ?o ?g. }
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- NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion type Assertion NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_head.
- NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion description "[Deficiencies of coagulation factors other than factor VIII and factor IX (afibrinogenemia, FII, FV, FV+FVIII, FVII, FX, FXI, FXIII) that cause bleeding disorders (RBDs) are inherited as autosomal recessive traits and are rare, with prevalences in the general population varying between 1 in 500,000 and 1 in 2 million for the homozygous forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_provenance.
- NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion evidence source_evidence_literature NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_provenance.
- NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion SIO_000772 16684009 NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_provenance.
- NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion wasDerivedFrom befree-20140225 NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_provenance.
- NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_assertion wasGeneratedBy ECO_0000203 NP327824.RADJbqMbm6WXyQoJKRCFix2QDCkMVED4Y5c_LN_f5fc2g130_provenance.