Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_assertion description "[Dystonia musculorum (dt) is an autosomal recessive hereditary neuropathy with a characteristic uncoordinated movement and is caused by a defect in the bullous pemphigoid antigen 1 (BPAG1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_assertion evidence source_evidence_literature NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_assertion SIO_000772 21272373 NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_assertion wasDerivedFrom befree-20140225 NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_assertion wasGeneratedBy ECO_0000203 NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210391.RA7lzeimO-P_hzWqhLKQZnIAlRuX9wrAwj2qoLFy-SwfY130_provenance.