Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_assertion description "[To determine the role of the single nucleotide polymorphism (SNP) (rs613872) in the TCF4 gene in Fuchs endothelial corneal dystrophy (FECD) in patients from Iowa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_assertion evidence source_evidence_literature NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_assertion SIO_000772 22998502 NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_assertion wasDerivedFrom befree-20140225 NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_assertion wasGeneratedBy ECO_0000203 NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP454208.RAo4ZDLH09dMZu1gGct6ywvq_AAtYgwPUIOMAJOv4-0l8130_provenance.