Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion description "[Disorders caused by mutations in the ARX gene include: hydrocephaly, lissencephaly and agenesis of corpus callosum with abnormal genitalia, Partington syndrome S), X-linked infantile spasms, myoclonic epilepsy, and nonspecific mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion evidence source_evidence_literature NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion SIO_000772 18975239 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion wasDerivedFrom lhgdn-20090331 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion wasGeneratedBy ECO_0000203 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.