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- source_evidence_literature type ECO_0000212 NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_assertion description "[Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_assertion evidence source_evidence_literature NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_assertion SIO_000772 20456451 NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_assertion wasDerivedFrom gad-20150221 NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_assertion wasGeneratedBy ECO_0000203 NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP113061.RAd_60uoOTMnjG9m6zKPZsSsQQ4ETatl6BrtR99EQk5RY130_provenance.