Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_assertion description "[This study was conducted to report a family affected by benign hereditary chorea in which a large deletion including TTF1, PAX9, and other genes was identified and results in oligodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_assertion evidence source_evidence_literature NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_assertion SIO_000772 18445003 NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_assertion wasDerivedFrom befree-20150227 NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_assertion wasGeneratedBy ECO_0000203 NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP739366.RAqpZ9AMOtV27yzKqU35Rh9b_13vR6fA6x1QUT-Drf5V4130_provenance.