Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion> ?p ?o ?g. }
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- NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion type Assertion NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_head.
- NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion description "[The abnormal phenotypes of the Hspg2-/- skeleton are similar to those of thanatophoric dysplasia (TD) type I, which is caused by activating mutations in FGFR3 (refs 7, 8, 9), and to those of Fgfr3 gain-of-function mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion evidence source_evidence_literature NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion SIO_000772 10545953 NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion wasDerivedFrom befree-2016 NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_assertion wasGeneratedBy ECO_0000203 NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.