Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• 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.
• NP468666.RATjff5B_vTiX98NemRfFFY2Ex3eUk4mz5QGhH0DKe7AA130_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." NP468666.RATjff5B_vTiX98NemRfFFY2Ex3eUk4mz5QGhH0DKe7AA130_provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP260386.RA-0a8cttdAggXFo72mKonUlFAeO5F_vYTFCKqlYQiaWE130_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." NP260386.RA-0a8cttdAggXFo72mKonUlFAeO5F_vYTFCKqlYQiaWE130_provenance.
• NP392782.RAdoP4a5PxolrYqzWt8R53S-kvIpu8SfiSbcEz_QXoJjo130_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." NP392782.RAdoP4a5PxolrYqzWt8R53S-kvIpu8SfiSbcEz_QXoJjo130_provenance.
• NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_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." NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_provenance.
• NP548802.RAWiIAqGunGzAIHPQHFsWplAWFO_5W5Esgo7MxCjV9KU4130_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." NP548802.RAWiIAqGunGzAIHPQHFsWplAWFO_5W5Esgo7MxCjV9KU4130_provenance.
• NP548805.RAY_VaymxTUOe4oA22tfdYJgiN50a3rXs6VHnJ_YGpreg130_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." NP548805.RAY_VaymxTUOe4oA22tfdYJgiN50a3rXs6VHnJ_YGpreg130_provenance.
• NP322830.RA3o6-suufMdSp_oJQRQkNAwabCHnlDEMuzwwrNd2DVgg130_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." NP322830.RA3o6-suufMdSp_oJQRQkNAwabCHnlDEMuzwwrNd2DVgg130_provenance.
• NP392245.RALoimqVH59VSYJqENUvkz9jlUGBsFlW0eMlHw3_IqFGc130_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." NP392245.RALoimqVH59VSYJqENUvkz9jlUGBsFlW0eMlHw3_IqFGc130_provenance.
• NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_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." NP548804.RAxVn3tMI40AuDtLXeCqyqJ3EfcV70OBKD3VGvigRTVRM130_provenance.