Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_assertion description "[We postulate that mutation of UMOD disrupts the tertiary structure of UMOD and is responsible for the clinical changes of interstitial renal disease, polyuria, and hyperuricaemia found in MCKD2 and FJHN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_assertion evidence source_evidence_literature NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_assertion SIO_000772 12471200 NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_assertion wasDerivedFrom befree-20140225 NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_assertion wasGeneratedBy ECO_0000203 NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP903045.RAaKKRD1GE3AVA4XfPkEhcFScnY4HDAHag_yfYIrBaJo4130_provenance.