Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion> ?p ?o ?g. }
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- NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion type Assertion NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_head.
- NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion description "[Therefore, we concluded that mutations of IDH are uncommon in ALL and OSCC and are apparently not a major consideration when selecting treatment modalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_provenance.
- NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion evidence source_evidence_literature NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_provenance.
- NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion SIO_000772 22385606 NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_provenance.
- NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion wasDerivedFrom befree-20140225 NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_provenance.
- NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_assertion wasGeneratedBy ECO_0000203 NP892960.RACRi1XaQMtKGRJVJLWuwNfqfbJPBge2tBUKrAkCNu_Pc130_provenance.