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- source_evidence_literature type ECO_0000212 NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_assertion description "[In the process of screening the above cohort of patients as well as other patients for CMT-causative mutations, we identified several previously unreported mutant alleles: two for connexin 32, three for myelin protein zero, and two for peripheral myelin protein 22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_assertion evidence source_evidence_literature NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_assertion SIO_000772 11835375 NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_assertion wasDerivedFrom gad-20150221 NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_assertion wasGeneratedBy ECO_0000203 NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72853.RAkivsMDF_nTUg-mHiL92-wa2J1JoeL0baYvSOmoMLPUY130_provenance.