Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP295012.RA7e7HauH9Jil9T98-vtUEc1aBge__oSvMbhP3guObmKY130_provenance.