Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion description "[Most probands have a congenital HL that is stable, symmetrical and without associated manifestations, but the audiometric profile should not be the only criteria for offering mutational screening of DFNB1 because of the observed variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion evidence source_evidence_literature NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion SIO_000772 18758381 NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion wasDerivedFrom befree-2016 NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion wasGeneratedBy ECO_0000203 NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.
- befree-2016 importedOn "2016-02-19" NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance.