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- source_evidence_literature type ECO_0000212 NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_assertion evidence source_evidence_literature NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_assertion SIO_000772 22178368 NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_assertion wasDerivedFrom befree-20150227 NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_assertion wasGeneratedBy ECO_0000203 NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674210.RAb_CttkzQuNa4MukajG4oxCZ70h4zCRJ-FHWf-ndZ-ZI130_provenance.