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- source_evidence_literature type ECO_0000212 NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_assertion evidence source_evidence_literature NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_assertion SIO_000772 10975746 NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_assertion wasDerivedFrom befree-20150227 NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_assertion wasGeneratedBy ECO_0000203 NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.