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- source_evidence_literature type ECO_0000212 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion description "[A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion evidence source_evidence_literature NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion SIO_000772 9040737 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion wasDerivedFrom befree-2016 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion wasGeneratedBy ECO_0000203 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- befree-2016 importedOn "2016-02-19" NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.