Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_assertion description "[Asymmetric phenotype of Axenfeld-Rieger anomaly and aniridia associated with a novel PITX2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_assertion evidence source_evidence_literature NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_assertion SIO_000772 21617748 NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_assertion wasDerivedFrom befree-20150227 NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_assertion wasGeneratedBy ECO_0000203 NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626424.RAVQJOkLR8BSvArseDMkVG8wA0mL8HWx-z_YlBD9ZLh-o130_provenance.