Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_assertion description "[This IL1RN SNP tags three other variants, none of which have previously been reported to be associated with renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_assertion evidence source_evidence_literature NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_assertion SIO_000772 20551628 NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_assertion wasDerivedFrom befree-2016 NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_assertion wasGeneratedBy ECO_0000203 NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.
- befree-2016 importedOn "2016-02-19" NP819137.RAq74q5MBv7xVYX0EwZ1kd4TBgv8JMRQgxyMI9IN1IHt4130_provenance.