Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_assertion description "[ARX gene mutations have been known as important causes of developmental and neurological disorders and are responsible for a large spectrum of abnormal phenotypes, includeing syndromic as well as nonsyndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_assertion evidence source_evidence_literature NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_assertion SIO_000772 16845484 NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_assertion wasDerivedFrom befree-20150227 NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_assertion wasGeneratedBy ECO_0000203 NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835494.RAXSDJSk733mQyzeLHag39Pjl4opg6l7gcVzRICPsEmZI130_provenance.