Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_assertion description "[In 288 children with ALL, cellular ASNS expression was more likely to be high in T-lineage ALL and low in B-lineage ALL with TEL-AML1 or hyperdiploidy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_assertion evidence source_evidence_literature NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_assertion SIO_000772 17380207 NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_assertion wasDerivedFrom befree-2016 NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_assertion wasGeneratedBy ECO_0000203 NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.
- befree-2016 importedOn "2016-02-19" NP600612.RAm6iOqV3_O66rIT0aBlu8hl_ugYP_Gphmj3CUTo1ROPc130_provenance.