Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion> ?p ?o ?g. }
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- NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion type Assertion NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_head.
- 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.
- NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion evidence source_evidence_literature NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_provenance.
- NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion SIO_000772 19563498 NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_provenance.
- NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion wasDerivedFrom befree-20140225 NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_provenance.
- NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_assertion wasGeneratedBy ECO_0000203 NP836327.RANetU90wci2vXr2wSHk8rlJz5A0GmLt4BZnk8JTlhrg8130_provenance.