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- source_evidence_literature type ECO_0000212 NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_assertion description "[While recessive mutations in RNF168 cause RIDDLE syndrome, an immune deficiency and radiosensitivity disorder, the potential impact of heterozygous deletion of RNF168 on patients with the 3q29 deletion syndrome is still unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_assertion evidence source_evidence_literature NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_assertion SIO_000772 21626679 NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_assertion wasDerivedFrom befree-2016 NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_assertion wasGeneratedBy ECO_0000203 NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.
- befree-2016 importedOn "2016-02-19" NP898217.RAZq5alEL6dMuneHXFdXAMdWD_Ce70pOrbE0PnirZiSm0130_provenance.