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- source_evidence_literature type ECO_0000212 NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_assertion description "[A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_assertion evidence source_evidence_literature NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_assertion SIO_000772 25652355 NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_assertion wasDerivedFrom befree-2016 NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_assertion wasGeneratedBy ECO_0000203 NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1261059.RA9nuwUBbNAYBkEKbN8567G52acsHQSn0b4zAoMIHgKgo130_provenance.