Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_assertion> ?p ?o ?g. }
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- NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_assertion type Assertion NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_head.
- NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_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." NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_provenance.
- NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_assertion evidence source_evidence_literature NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_provenance.
- NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_assertion SIO_000772 22319038 NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_provenance.
- NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_assertion wasDerivedFrom befree-20150227 NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_provenance.
- NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_assertion wasGeneratedBy ECO_0000203 NP400494.RAn6nuWrtE7oRoY_LoXYP2NPSQKB0u2zFV7SXv5yHVJC8130_provenance.