Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP266748.RA3BE8CPwvt8lPg8zfeJ0o_XM0Yn_fomq70dGcJ5UIh2A130_provenance.