Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_assertion description "[We have mapped this gene to the 3 Mb critical region of gene loss of the 5q- syndrome within 5q32, flanked by the genes for ADRB2 and IL12B, using gene dosage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_assertion evidence source_evidence_literature NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_assertion SIO_000772 10982193 NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_assertion wasDerivedFrom befree-20140225 NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_assertion wasGeneratedBy ECO_0000203 NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP782251.RAx04sfwnGFbuoj6FFyrjqwMaGXdzwgIkhSmLHxTMgNpY130_provenance.