Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_assertion> ?p ?o ?g. }
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- NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_assertion type Assertion NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_head.
- NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_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." NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_provenance.
- NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_assertion evidence source_evidence_literature NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_provenance.
- NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_assertion SIO_000772 22319038 NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_provenance.
- NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_assertion wasDerivedFrom befree-20140225 NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_provenance.
- NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_assertion wasGeneratedBy ECO_0000203 NP576314.RAFX2Y7u6Ik44IksmtzIlec-7WEPqcT01K1fLFKtSHhRA130_provenance.