Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion wasGeneratedBy ECO_0000203 NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion wasDerivedFrom befree-20140225 NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion SIO_000772 9541114 NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion evidence source_evidence_literature NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.