Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_assertion description "[Cases 3 and 4, two siblings with a novel variant in ARX, which is not clearly pathogenic, have developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_assertion evidence source_evidence_literature NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_assertion SIO_000772 18462864 NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_assertion wasDerivedFrom befree-20150227 NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_assertion wasGeneratedBy ECO_0000203 NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835532.RAf0wrRpoaRuZgb_6x9_Kbj1Lu1owl7_FA09nT5oEiswY130_provenance.