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- source_evidence_literature type ECO_0000212 NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_assertion description "[This suggested that the ability to stabilize the UPF3A protein is a crucial modifier of the neurological symptoms due to loss of UPF3B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_assertion evidence source_evidence_literature NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_assertion SIO_000772 22182939 NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_assertion wasDerivedFrom befree-20150227 NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_assertion wasGeneratedBy ECO_0000203 NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941099.RABMCHQU6mf4XGgm_24EYLU6ZsRQ5idh7oKLI-bRohS9o130_provenance.