Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion type Assertion NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_head.
- NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion description "[A total of 103 patients with either CPHD (n = 35) or SOD (n = 68) were investigated for mutations in genes implicated in the etiology of KS (FGFR1, FGF8, PROKR2, PROK2, and KAL1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_provenance.
- NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion evidence source_evidence_literature NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_provenance.
- NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion SIO_000772 22319038 NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_provenance.
- NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion wasDerivedFrom befree-2016 NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_provenance.
- NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_assertion wasGeneratedBy ECO_0000203 NP959586.RAKqGXbrBWnmCCLLJrhXhbAPCEKJxopgP1pV5JbCovM-o130_provenance.