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- source_evidence_literature type ECO_0000212 NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- befree-2016 importedOn "2016-02-19" NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_assertion wasGeneratedBy ECO_0000203 NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_assertion wasDerivedFrom befree-2016 NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_assertion SIO_000772 18666230 NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_assertion evidence source_evidence_literature NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.
- NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_assertion description "[Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685076.RA2bL-t2QmYDgeWqsG_bXmR0Z_Eb6NAS2wngFWTnNBm9A130_provenance.