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- source_evidence_literature type ECO_0000212 NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_assertion description "[Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_assertion evidence source_evidence_literature NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_assertion SIO_000772 15565467 NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_assertion wasDerivedFrom befree-2016 NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_assertion wasGeneratedBy ECO_0000203 NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP470368.RAZmzPUJ2BychitJyUKXD6x-KFZj4VmoPf5zc4ETx3E8Y130_provenance.