Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_assertion description "[Mutated MID1, as found in OS patients, loses its influence on MIDAS-containing mRNAs, suggesting that the malformations in OS patients could be caused by failures in the regulation of cytoskeleton-bound protein translation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_assertion evidence source_evidence_literature NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_assertion SIO_000772 21930711 NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_assertion wasDerivedFrom befree-2016 NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_assertion wasGeneratedBy ECO_0000203 NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.
- befree-2016 importedOn "2016-02-19" NP924776.RAEq2MAmJ6lS1tu4aO2BHUzrPlMPBu7_81Y7--YLMSAgk130_provenance.