Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion> ?p ?o ?g. }
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- NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_assertion type Assertion NP79979.RA_GHDGY1S0NKMLDnYKgn3BV07x3AHIUHwSHgw3-mPLbg130_head.
- 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.