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- source_evidence_literature type ECO_0000212 NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_assertion description "[The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_assertion evidence source_evidence_literature NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_assertion SIO_000772 10732799 NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_assertion wasDerivedFrom befree-2016 NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_assertion wasGeneratedBy ECO_0000203 NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.
- befree-2016 importedOn "2016-02-19" NP278920.RAYTY9FSVNn1S6-yehz8Zxg4KzIcEuSolP9aKtHIGfnI4130_provenance.