Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion> ?p ?o ?g. }
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- NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion type Assertion NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_head.
- NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion description "[Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_provenance.
- NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion evidence source_evidence_literature NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_provenance.
- NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion SIO_000772 21889209 NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_provenance.
- NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion wasDerivedFrom befree-20140225 NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_provenance.
- NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_assertion wasGeneratedBy ECO_0000203 NP837731.RAF8aZClLDlICrzKnPyXcfFnf_a4QyhI9X12Ls1sbzquY130_provenance.