Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_assertion description "[Charcot-Marie-Tooth neuropathy (CMT) type 1 is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (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." NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_assertion evidence source_evidence_literature NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_assertion SIO_000772 7804455 NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_assertion wasDerivedFrom befree-2016 NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_assertion wasGeneratedBy ECO_0000203 NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1322379.RA1jon23yB_jVQClNzs5XQBKEKAMzAXWCbBuqrRhOQSgM130_provenance.