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- source_evidence_literature type ECO_0000212 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion wasGeneratedBy ECO_0000203 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion wasDerivedFrom befree-20140225 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion SIO_000772 15776429 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion evidence source_evidence_literature NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion description "[We screened the SIMPLE gene for mutations in a cohort of 192 patients with CMT or related neuropathies, each of whom tested negative for other known genetic causes of CMT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.