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- source_evidence_literature type ECO_0000212 NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_assertion description "[Biofluid studies identify about 15% of patients with FTLD due to a genetic mutation that is associated with the specific histopathologic features of TDP-43 or a tauopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_assertion evidence source_evidence_literature NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_assertion SIO_000772 21833654 NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_assertion wasDerivedFrom befree-20150227 NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_assertion wasGeneratedBy ECO_0000203 NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872886.RAA3r5BOLRIuRNls_ez_nKFdZ-r6mIbwEzC-0Wet-izi0130_provenance.