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- source_evidence_literature type ECO_0000212 NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_assertion description "[Dejerine-Sottas disease, also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene of the P0 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_assertion evidence source_evidence_literature NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_assertion SIO_000772 7849745 NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_assertion wasDerivedFrom befree-2016 NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_assertion wasGeneratedBy ECO_0000203 NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1323786.RAkesMjl-VC-CzjsNCqTmxi_-jFc_oZbYo8PEdo1WqTbw130_provenance.