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- source_evidence_literature type ECO_0000212 NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_assertion evidence source_evidence_literature NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_assertion SIO_000772 21990111 NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_assertion wasDerivedFrom befree-20140225 NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_assertion wasGeneratedBy ECO_0000203 NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP325314.RAuDNPjse_1AN7TTje9pNTD522_SRGkYzHwfS5pv2qdFo130_provenance.