Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_assertion description "[In addition, no pathogenic sequence variations were found in DCN, DSPG3, LUM, PITX2 and FOXC1, which have also been implicated in corneal and anterior segment dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_assertion evidence source_evidence_literature NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_assertion SIO_000772 17558846 NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_assertion wasDerivedFrom befree-2016 NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_assertion wasGeneratedBy ECO_0000203 NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP614328.RA4yknrh5gyiW0w-LP-VwjeZZRa5tNwhRzKL3oCthyJpQ130_provenance.