Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion> ?p ?o ?g. }
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- NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion type Assertion NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_head.
- NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion description "[FGFR3 mutations appear to be common genetic alterations in multiple SK with a varying interindividual mutation frequency but without specific intraindividual hot spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_provenance.
- NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion evidence source_evidence_literature NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_provenance.
- NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion SIO_000772 17392824 NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_provenance.
- NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion wasDerivedFrom befree-20140225 NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_provenance.
- NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_assertion wasGeneratedBy ECO_0000203 NP373793.RAGV9nr1Ni8UW9mwLAVvbAqzJZA52LLq0OgZccLevsLGc130_provenance.