Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_assertion description "[Two brothers with no copy of Cx32, 27 and 25 years old, showed steppage gait, moderate muscle atrophy and weakness, and mild sensory disturbance in the distal parts of the legs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_assertion evidence source_evidence_literature NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_assertion SIO_000772 11266688 NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_assertion wasDerivedFrom befree-20140225 NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_assertion wasGeneratedBy ECO_0000203 NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP936409.RA8n2pthCvsNKC2rwqq5kMjy_hm_QU7hDxUs9pEKKQT-k130_provenance.