Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_assertion wasGeneratedBy ECO_0000203 NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_assertion wasDerivedFrom gad-20150221 NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_assertion SIO_000772 20198651 NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_assertion evidence source_evidence_literature NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.
- NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_assertion description "[The aim of this study was to characterize the FOXL2 mutation in human tumour tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149892.RAEIJnH4eXRjfZgbZT9akhnEqxZAVJdgxpe7h_pu5tF2c130_provenance.