Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion wasGeneratedBy ECO_0000203 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion wasDerivedFrom befree-2016 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion SIO_000772 23163601 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion evidence source_evidence_literature NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.