Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_assertion description "[PAX6 mutations may be associated with diverse clinical features ranging from severely impaired ocular and pituitary development to apparently normal phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_assertion evidence source_evidence_literature NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_assertion SIO_000772 25342853 NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_assertion wasDerivedFrom befree-20150227 NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_assertion wasGeneratedBy ECO_0000203 NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP610436.RAuThV_dFoer6rm-ZTqCvSDc4A4NRPo907SdUIC7SiYvw130_provenance.