Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion description "[Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion evidence source_evidence_literature NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion SIO_000772 18452394 NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion wasDerivedFrom gad-20130706 NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion wasGeneratedBy ECO_0000203 NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_provenance.