Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_assertion wasGeneratedBy ECO_0000203 NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_assertion wasDerivedFrom befree-20150227 NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_assertion SIO_000772 22534615 NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_assertion evidence source_evidence_literature NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.
- NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_assertion description "[In this family, a T613M mutation in the ATP1A3 gene was confirmed, the most common mutation present in patients with RDP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256186.RAqF6HB9_5vWv3S9iJW4hl4rvXKdTS28lJJacrsW2Hw7c130_provenance.