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- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion type Assertion NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_head.
- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_provenance.
- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion evidence source_evidence_literature NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_provenance.
- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion SIO_000772 19506355 NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_provenance.
- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion wasDerivedFrom befree-20140225 NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_provenance.
- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion wasGeneratedBy ECO_0000203 NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_provenance.