Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_assertion description "[Even among family members with a single TBX1 point mutation but no cytological deletion, cleft palate and low-set ears may or may not be present.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_assertion evidence source_evidence_literature NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_assertion SIO_000772 19247433 NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_assertion wasDerivedFrom befree-20140225 NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_assertion wasGeneratedBy ECO_0000203 NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP778515.RAFka9ZZRWd3yGWfVTtqzwcufKOfqs6QSPdevDkqZFxYY130_provenance.