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- source_evidence_literature type ECO_0000212 NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_assertion description "[To assess the genetic association of transcription factor 4 (TCF4) intronic polymorphisms and CTG18.1 allele in individuals with Fuchs' endothelial corneal dystrophy (FECD) individuals from a sample Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_assertion evidence source_evidence_literature NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_assertion SIO_000772 25342617 NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_assertion wasDerivedFrom befree-2016 NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_assertion wasGeneratedBy ECO_0000203 NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232313.RAD0Xy_bfRwltYPruSqKfqVLzzU0iOwmASZfYmjh1miOQ130_provenance.