Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion> ?p ?o ?g. }
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- NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion type Assertion NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_head.
- NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion description "[Alterations of known genes in PRCC include missense mutations in the MET oncogene (7q31) and rare translocations fusing TFE3 at Xp11.2 with a variety of other loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_provenance.
- NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion evidence source_evidence_literature NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_provenance.
- NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion SIO_000772 12213728 NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_provenance.
- NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion wasDerivedFrom befree-2016 NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_provenance.
- NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_assertion wasGeneratedBy ECO_0000203 NP366945.RAkRQh2GmJxuf1j7uWQ2pi-oR5peYAhFTZa0PSJT08apI130_provenance.