Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_assertion description "[Investigation of a PAX6 gene mutation in a Malaysian family with congenital aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_assertion evidence source_evidence_literature NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_assertion SIO_000772 24737507 NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_assertion wasDerivedFrom befree-20150227 NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_assertion wasGeneratedBy ECO_0000203 NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP610295.RAdeVdsUGI3-Nmi8_EIcrUkyTIp13NFqmhE88t3C84IOM130_provenance.