Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_assertion description "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_assertion evidence source_evidence_literature NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_assertion SIO_000772 18554165 NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_assertion wasDerivedFrom gad-20130706 NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_assertion wasGeneratedBy ECO_0000203 NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP74440.RAoO6nnNfNjzBUSO9MTZtaQy3r1tXnjpdJUMGIgBiHToo130_provenance.