Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_assertion description "[Furthermore, our results strongly support the concept that PMP22-related neuropathies (and most likely also other forms of inherited motor and sensory neuropathies) should be viewed as the consequence of impaired neuron-Schwann cell interactions that are likely already to be operative during development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_assertion evidence source_evidence_literature NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_assertion SIO_000772 10586249 NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_assertion wasDerivedFrom befree-2016 NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_assertion wasGeneratedBy ECO_0000203 NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP269204.RARVfHFEMJy_o8VfWWtsy0bO6EFTz9igUv6A9KPMmwmQQ130_provenance.