Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion type Assertion NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_head.
- NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion description "[No rearrangements or deletions of the INK4d gene were observed in Southern blot analysis of selected cases of pediatric acute lymphoblastic leukemia (ALL) containing a variant (1;19)(q23;p13) translocation that lacks rearrangement of either E2A or PBX1, or in ALL cases containing homozygous or hemizygous deletions of the related genes, INK4a and INK4b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion evidence source_evidence_literature NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion SIO_000772 8575754 NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion wasDerivedFrom befree-20140225 NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_assertion wasGeneratedBy ECO_0000203 NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.