Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17p (CMT1A), chromosome 1q (CMT1B), the X chromosome (CMTX) and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_assertion evidence source_evidence_literature NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_assertion SIO_000772 7952853 NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_assertion wasDerivedFrom befree-2016 NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_assertion wasGeneratedBy ECO_0000203 NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1328094.RAicQiddj5MwsNMdc-KZO2sZJnZ0M_yfoA5RmcqYAZkk0130_provenance.