Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_assertion description "[A total of 45 unrelated patients with GT were enrolled in the present study to identify the causative molecular defects, and also to correlate their phenotype with their genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_assertion evidence source_evidence_literature NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_assertion SIO_000772 19691478 NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_assertion wasDerivedFrom befree-2016 NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_assertion wasGeneratedBy ECO_0000203 NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.
- befree-2016 importedOn "2016-02-19" NP758402.RAzg6elGkhowjuVff2gxeSAVZhqYlezvuaJ_BeLH568i8130_provenance.