Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion> ?p ?o ?g. }
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- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion type Assertion NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_head.
- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion description "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_provenance.
- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion evidence source_evidence_literature NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_provenance.
- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion SIO_000772 19506355 NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_provenance.
- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion wasDerivedFrom befree-20150227 NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_provenance.
- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion wasGeneratedBy ECO_0000203 NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_provenance.