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- source_evidence_literature type ECO_0000212 NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_assertion description "[The data expand the clinical spectrum of TH deficiency and suggest that TH mutations may account for some patients with DRD simulating spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_assertion evidence source_evidence_literature NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_assertion SIO_000772 11160968 NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_assertion wasDerivedFrom befree-20150227 NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_assertion wasGeneratedBy ECO_0000203 NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP735395.RASHnfdUhJKc0dnbz4mWlF0fGj_t0TjAYs_ptfQtn3INc130_provenance.