Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_assertion description "[Homozygous deletions may be markers of nearby heterozygous mutations: The complex deletion at FRA16D in the HCT116 colon cancer cell line removes exons of WWOX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_assertion evidence source_evidence_literature NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_assertion SIO_000772 18273838 NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_assertion wasDerivedFrom befree-2016 NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_assertion wasGeneratedBy ECO_0000203 NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.
- befree-2016 importedOn "2016-02-19" NP655365.RApSJLAG5ldWvWoel7NdmjMGYu_2Yyv1eh0viqaDbIMRk130_provenance.