Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_assertion> ?p ?o ?g. }
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- NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_assertion type Assertion NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_head.
- NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_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." NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_provenance.
- NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_assertion evidence source_evidence_literature NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_provenance.
- NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_assertion SIO_000772 12213728 NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_provenance.
- NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_assertion wasDerivedFrom befree-20140225 NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_provenance.
- NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_assertion wasGeneratedBy ECO_0000203 NP166124.RAmd68f6S5Rmgccc2FmWdkYieAWdzHmShlqNepJ_uMkn0130_provenance.