Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_assertion description "[The NR2 hybrid allowed us to exclude three candidate genes for AGS: hepatic nuclear factor 3 beta (HNF3 beta), paired box 1 (PAX1), and cystatin C (CST3) as shown by their localization outside of the deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_assertion evidence source_evidence_literature NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_assertion SIO_000772 7873876 NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_assertion wasDerivedFrom befree-2016 NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_assertion wasGeneratedBy ECO_0000203 NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1324458.RAJiAfmFthkmAiWU0p7kao1dn21BSN74RFnuhY5nSabA4130_provenance.