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- NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_assertion type Assertion NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_head.
- NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_assertion description "[Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_provenance.
- NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_assertion evidence source_evidence_literature NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_provenance.
- NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_assertion SIO_000772 19066959 NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_provenance.
- NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_assertion wasDerivedFrom befree-2016 NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_provenance.
- NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_assertion wasGeneratedBy ECO_0000203 NP708098.RAVrbGandd3vN7B2QXVNc_FBBGIc2mQ0FGgTv0RJ1KJew130_provenance.