Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_assertion description "[Mutations interact with NPHS2 protein to produce either nephrotic syndrome or focal glomerosclerosis, depending on alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_assertion evidence source_evidence_literature NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_assertion SIO_000772 11854170 NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_assertion wasDerivedFrom lhgdn-20090331 NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_assertion wasGeneratedBy ECO_0000203 NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193326.RAAXUQh4FAyuPijLw8yu65BgVWyMxCoSx_-Y5wI6Oxg7I130_provenance.