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- source_evidence_literature type ECO_0000212 NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_assertion description "[A molecular study has revealed a novel missense mutation, T614I, in exon 17 of SPG4, which may play a role in both focal cortical dysgenesis and neurodegeneration of the motor neurons in the corticospinal tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_assertion evidence source_evidence_literature NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_assertion SIO_000772 15159500 NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_assertion wasDerivedFrom befree-20150227 NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_assertion wasGeneratedBy ECO_0000203 NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710031.RALJ8esuvSE39MZK5uNujnbHa2IiqDBBz1dLwmTsyort8130_provenance.