Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_assertion description "[In 1994, the field of bone biology was significantly advanced by the discovery that activating mutations in the fibroblast growth factor receptor 3 (FGFR3) receptor tyrosine kinase (TK) account for the common genetic form of dwarfism in humans, achondroplasia (ACH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_assertion evidence source_evidence_literature NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_assertion SIO_000772 22045636 NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_assertion wasDerivedFrom befree-2016 NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_assertion wasGeneratedBy ECO_0000203 NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.
- befree-2016 importedOn "2016-02-19" NP935450.RASMyv-FIkl28e4nqbZdBhEn6We0mwWWTO8GEnzlL5BEw130_provenance.