Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_assertion description "[The G380R mutation in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) causes achondroplasia, the most common form of human dwarfism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_assertion evidence source_evidence_literature NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_assertion SIO_000772 21324899 NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_assertion wasDerivedFrom befree-20150227 NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_assertion wasGeneratedBy ECO_0000203 NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.