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- source_evidence_literature type ECO_0000212 NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_assertion description "[Haplotypic analysis of three Rieger syndrome regions in a large family with Axenfeld-Rieger syndrome excluded linkage to the 4q25 (PITX2), 6p25 (FOXC1), and 13q14 (RIEG2) regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_assertion evidence source_evidence_literature NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_assertion SIO_000772 11821690 NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_assertion wasDerivedFrom befree-20150227 NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_assertion wasGeneratedBy ECO_0000203 NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626408.RAZX5yglYM6hqz5lAh-6nbi6ajMgDwIdUi42daT4pg6QA130_provenance.