Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_assertion description "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_assertion evidence source_evidence_literature NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_assertion SIO_000772 18379723 NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_assertion wasDerivedFrom befree-20150227 NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_assertion wasGeneratedBy ECO_0000203 NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426100.RAKUZp-cj32ePrlyZjDBhcj8vVkwF-MbAWeqtqVac7HO0130_provenance.