Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion description "[X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion evidence source_evidence_literature NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion SIO_000772 21291455 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion wasDerivedFrom befree-2016 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_assertion wasGeneratedBy ECO_0000203 NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.
- befree-2016 importedOn "2016-02-19" NP869995.RAo0H8Eps-IM9kVDkKvH5p0IdCo-OLdD779eymfJEGdH8130_provenance.