Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_assertion description "[We propose that the microcephaly observed in patients with MCPH1 deficiencies is due to disruption of the ATR-BRCA1-Chk1 signaling pathway that is also disrupted in Seckel syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_assertion evidence source_evidence_literature NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_assertion SIO_000772 16217032 NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_assertion wasDerivedFrom befree-20140225 NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_assertion wasGeneratedBy ECO_0000203 NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP350287.RA5pn4sKqtiCFMFQPm0RoO029aMWTT1tPevqB_HLJkXrM130_provenance.