Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_assertion> ?p ?o ?g. }
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- NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_assertion type Assertion NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_head.
- NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_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." NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_provenance.
- NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_assertion evidence source_evidence_literature NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_provenance.
- NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_assertion SIO_000772 12213728 NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_provenance.
- NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_assertion wasDerivedFrom befree-20140225 NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_provenance.
- NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_assertion wasGeneratedBy ECO_0000203 NP591392.RARkQVCu9fWQPKQaNLi6ebuATTy1x5tJmx6do6gN38YUg130_provenance.