Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_assertion description "[We describe a new variant of Bernard-Soulier syndrome characterized by almost normal amounts of GPIb and severely reduced GPIX and GPV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_assertion evidence source_evidence_literature NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_assertion SIO_000772 9886312 NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_assertion wasDerivedFrom befree-20140225 NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_assertion wasGeneratedBy ECO_0000203 NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP155138.RAATetbKt2_QYHMFvDfesk8yTQd1gJgRRMFVol9oh_0sQ130_provenance.