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- source_evidence_literature type ECO_0000212 NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_assertion wasGeneratedBy ECO_0000203 NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_assertion wasDerivedFrom befree-20150227 NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_assertion SIO_000772 21940684 NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_assertion evidence source_evidence_literature NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.