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- NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_assertion type Assertion NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_head.
- NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_assertion description "[FGFR1 and FGFR2 mutations in Pfeiffer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_provenance.
- NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_assertion evidence source_evidence_literature NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_provenance.
- NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_assertion SIO_000772 23348274 NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_provenance.
- NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_assertion wasDerivedFrom befree-2016 NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_provenance.
- NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_assertion wasGeneratedBy ECO_0000203 NP1046693.RAsYwlQl8goNioL0VDvTPhWaM5TiDSavMICnRgIui_vzM130_provenance.