Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_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." NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_assertion evidence source_evidence_literature NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_assertion SIO_000772 10545953 NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_assertion wasDerivedFrom befree-20150227 NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_assertion wasGeneratedBy ECO_0000203 NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP469953.RAQ4A0vR0_jybg-t96BrJO64RGADG278Sc2o8D-0TJNpY130_provenance.