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- source_evidence_literature type ECO_0000212 NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_assertion description "[Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_assertion evidence source_evidence_literature NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_assertion SIO_000772 11487566 NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_assertion wasDerivedFrom befree-2016 NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_assertion wasGeneratedBy ECO_0000203 NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.
- befree-2016 importedOn "2016-02-19" NP326082.RAvH4UMvd9Uasd-lA1tAlR6GtLYa5k7_VZKY3CGstywNk130_provenance.