Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_assertion description "[Interestingly, binding of both mutant receptors to FGF9 was notably enhanced and implicates FGF9 as a potential pathophysiological ligand for mutant FGFRs in mediating craniosynostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_assertion evidence source_evidence_literature NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_assertion SIO_000772 14613973 NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_assertion wasDerivedFrom befree-2016 NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_assertion wasGeneratedBy ECO_0000203 NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP420430.RAXj8S6-RWjojlZoXvI4cZx4cIHf_xabdsp6368EMDHOQ130_provenance.