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- source_evidence_literature type ECO_0000212 NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- befree-2016 importedOn "2016-02-19" NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_assertion wasGeneratedBy ECO_0000203 NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_assertion wasDerivedFrom befree-2016 NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_assertion SIO_000772 11575598 NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_assertion evidence source_evidence_literature NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.
- NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_assertion description "[We studied 3 members of a family who each had leukoencephalopathy on neuroimaging studies and a characteristic mutation for CADASIL in the notch 3 region of chromosome 19q12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331309.RAfiWJKh9Dk21szbwhxZRDcFiBiJ7b3EQfxX8-HO68SJs130_provenance.