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- source_evidence_literature type ECO_0000212 NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_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." NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_assertion evidence source_evidence_literature NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_assertion SIO_000772 18450588 NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_assertion wasDerivedFrom gad-20150221 NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_assertion wasGeneratedBy ECO_0000203 NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52001.RAeHDfOt2YjIKvY1qDOo-15HlmRX8L6EO2J4QjRyE3z-M130_provenance.