Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion> ?p ?o ?g. }
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- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion type Assertion NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_head.
- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion description "[In addition, the p.P252R mutation in FGFR1 was detected in 1 PS patient with unilateral coronal craniosynostosis expanding the phenotypic spectrum of PS with this particular mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_provenance.
- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion evidence source_evidence_literature NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_provenance.
- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion SIO_000772 23348274 NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_provenance.
- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion wasDerivedFrom befree-2016 NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_provenance.
- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion wasGeneratedBy ECO_0000203 NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_provenance.