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- source_evidence_literature type ECO_0000212 NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_assertion description "[Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_assertion evidence source_evidence_literature NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_assertion SIO_000772 25403472 NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_assertion wasDerivedFrom befree-2016 NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_assertion wasGeneratedBy ECO_0000203 NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238021.RAhYlEwPd0WQk4aO04h9E4w7ry-N0hyhch-K4dxLjnee0130_provenance.