Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_assertion description "[All together, our results indicate that mutations in IL1RAPL1 cause a spectrum of neurological impairments ranging from MR to high functioning autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_assertion evidence source_evidence_literature NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_assertion SIO_000772 18801879 NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_assertion wasDerivedFrom befree-20150227 NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_assertion wasGeneratedBy ECO_0000203 NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP860548.RAeG_wklZm06eUeW3Vs0IkCfViQL6YQ0slqbOLUHGNEg0130_provenance.