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- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion type Assertion NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_head.
- 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.