Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_assertion description "[Genetic analysis revealed a Wilms' tumour (WT1) gene mutation characteristic of the Frasier syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_assertion evidence source_evidence_literature NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_assertion SIO_000772 12932885 NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_assertion wasDerivedFrom befree-2016 NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_assertion wasGeneratedBy ECO_0000203 NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.
- befree-2016 importedOn "2016-02-19" NP406374.RAJlffOs9g7MxKrWSAeWEHtd9QZVBXhwU35xYFNIy12qM130_provenance.