Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion type Assertion NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_head.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_provenance.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion evidence source_evidence_literature NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_provenance.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion SIO_000772 12717434 NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_provenance.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion wasDerivedFrom befree-20140225 NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_provenance.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion wasGeneratedBy ECO_0000203 NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_provenance.