Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_assertion description "[ALDH1A3 mutations cause recessive anophthalmia and microphthalmia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_assertion evidence source_evidence_literature NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_assertion SIO_000772 23312594 NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_assertion wasDerivedFrom befree-20140225 NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_assertion wasGeneratedBy ECO_0000203 NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.
- befree-20140225 importedOn "2014-02-25" NP219172.RAnxbcTRT4mLv-yj_b3AaB00VOTVrmlTn2qgSVp2NRxog130_provenance.