Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_assertion description "[Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_assertion evidence source_evidence_literature NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_assertion SIO_000772 10762296 NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_assertion wasDerivedFrom befree-2016 NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_assertion wasGeneratedBy ECO_0000203 NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.
- befree-2016 importedOn "2016-02-19" NP280884.RAX0gjA5IFW1q1zNCFjmD75VX8S1Wd4QWSkFYDsPyV0rg130_provenance.