Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_assertion description "[Thus the ability to activate STAT1 appears restricted to the K650M and K650E-FGFR3 mutants, which however account for only a small minority of the FGFR3-related skeletal dysplasia cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_assertion evidence source_evidence_literature NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_assertion SIO_000772 19088846 NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_assertion wasDerivedFrom befree-20140225 NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_assertion wasGeneratedBy ECO_0000203 NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP420779.RAuOtv7GNLvuQcXC5WfmLHYYcBc5_P_jGFnOu9LfHjjW4130_provenance.