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- source_evidence_literature type ECO_0000212 NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_assertion description "[In the present study an FSCN2 mutation was examined that has been reported, not only in patients with retinitis pigmentosa (RP), but also in the normal population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_assertion evidence source_evidence_literature NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_assertion SIO_000772 18450588 NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_assertion wasDerivedFrom befree-2016 NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_assertion wasGeneratedBy ECO_0000203 NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP668840.RAtCFsncqZ1mc4Hqwow9y642k32_tty1GDeqSQAo7dwQ4130_provenance.