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- source_evidence_literature type ECO_0000212 NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_assertion description "[We aimed to characterize genotype-phenotype correlations and establish baseline clinical data for peripheral neuropathies caused by mutations in the myelin protein zero (MPZ) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_assertion evidence source_evidence_literature NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_assertion SIO_000772 26310628 NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_assertion wasDerivedFrom befree-2016 NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_assertion wasGeneratedBy ECO_0000203 NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293244.RAhm3AlX_bhA2UPh21cwFALPrjzcM78G-Oj8hlaOsUcCI130_provenance.