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- source_evidence_literature type ECO_0000212 NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_assertion wasGeneratedBy ECO_0000203 NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_assertion wasDerivedFrom befree-2016 NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_assertion SIO_000772 8128981 NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_assertion evidence source_evidence_literature NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.
- NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_assertion description "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.