Matches in Nanopublications for { ?s ?p "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP254559.RAdxWMAUreXJ8330zRzBb0W_pxxepVd7hvWtZa7NKcij4130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254559.RAdxWMAUreXJ8330zRzBb0W_pxxepVd7hvWtZa7NKcij4130_provenance.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_provenance.
- NP218505.RArx8o-DfZMjNyNnAygGCfJzEXyJ83oMCL2js9QYmY0RA130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218505.RArx8o-DfZMjNyNnAygGCfJzEXyJ83oMCL2js9QYmY0RA130_provenance.
- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- NP777128.RA9tyDScrtjJecrud4kfdaaAtgqgmEsAL7g02bZ5oNeC8130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777128.RA9tyDScrtjJecrud4kfdaaAtgqgmEsAL7g02bZ5oNeC8130_provenance.
- NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_provenance.