Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_assertion description "[Our results confirm the significant contribution of ARX mutations in the etiology of MR, especially in this group of patients selected for XLMR (3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_assertion evidence source_evidence_literature NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_assertion SIO_000772 16523516 NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_assertion wasDerivedFrom befree-2016 NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_assertion wasGeneratedBy ECO_0000203 NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.
- befree-2016 importedOn "2016-02-19" NP539172.RAuS2vJwEixxMlhaU_JOQ40ofCLpERJw0Ao01ByM7gXrM130_provenance.