Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_assertion description "[An A-to-G mutation at the +3 position of intron 8 of the HEXA gene is associated with exon 8 skipping and Tay-Sachs disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_assertion evidence source_evidence_literature NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_assertion SIO_000772 7551830 NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_assertion wasDerivedFrom gad-20130706 NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_assertion wasGeneratedBy ECO_0000203 NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP60384.RAiwFfPeMabcTKF-LtNRFZEaFgMEryBqnHMQlpIySnilY130_provenance.