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- source_evidence_literature type ECO_0000212 NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_assertion description "[Our findings suggest that SCN1A mutations may cause susceptibility to an idiopathic focal epilepsy phenotype, the final phenotype depending on other (genetic or nongenetic) factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_assertion evidence source_evidence_literature NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_assertion SIO_000772 19339291 NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_assertion wasDerivedFrom befree-20140225 NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_assertion wasGeneratedBy ECO_0000203 NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.