Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_assertion description "[Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_assertion evidence source_evidence_curated NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_assertion SIO_000772 11850618 NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_assertion wasDerivedFrom uniprot-20130724 NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_assertion wasGeneratedBy ECO_0000218 NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6610.RAaFuwNVe_yki667BB9wsW2qC2_-blsVBM6ir_xI3K_Hw130_provenance.