Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion> ?p ?o ?g. }
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- NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion type Assertion NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_head.
- NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion description "[We analyzed a series of sporadic type 1 and type 2 PRCC cases for MET mutations, TFE3 rearrangements, and allelic imbalance (AI) on 3p, 6, 7q, 9p, 11, 13q, 14q, 17q, 18, 20q, and 21q and compared selected results with a series of conventional renal cell carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_provenance.
- NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion evidence source_evidence_literature NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_provenance.
- NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion SIO_000772 12213728 NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_provenance.
- NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion wasDerivedFrom befree-20150227 NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_provenance.
- NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_assertion wasGeneratedBy ECO_0000203 NP802799.RARXQ4XGisxr0Q4UQXHIDS-aBGEljHCc7lUPbNmRIoi6Q130_provenance.