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- source_evidence_literature type ECO_0000212 NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_assertion description "[A novel MPZ mutation in Charcot-Marie-Tooth disease type 1B with focally folded myelin and multiple entrapment neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_assertion evidence source_evidence_literature NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_assertion SIO_000772 21940171 NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_assertion wasDerivedFrom befree-20150227 NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_assertion wasGeneratedBy ECO_0000203 NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568184.RAR3m_cpJZHHsNq2Xj5AkIdQx3rmhMbN636iv-DbdEvpQ130_provenance.