Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion> ?p ?o ?g. }
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- NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion type Assertion NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_head.
- NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion wasGeneratedBy ECO_0000203 NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_provenance.
- NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion wasDerivedFrom befree-20140225 NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_provenance.
- NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion SIO_000772 9212218 NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_provenance.
- NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion evidence source_evidence_literature NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_provenance.
- NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_assertion description "[The relatively low rate of p16 mutation observed here coupled with the high frequency of loss of heterozygosity on chromosome 9 suggests that one or several tumor-suppressor gene(s) distinct from p16 may be the target(s) of allelic deletion in most esophageal cancers or that p16 is inactivated in another way.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430688.RAKMaiHIFxkRrUt8vlDPohPwj2GZ4UWU78pKItBpM6ngw130_provenance.