Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_assertion description "[The cell line established from nodule (SCID 5019 p11), showed a number of new changes, as described; however, the most significant change was amplification of the 8q23 approximately qter region, harboring c-myc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_assertion evidence source_evidence_literature NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_assertion SIO_000772 10942801 NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_assertion wasDerivedFrom befree-20140225 NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_assertion wasGeneratedBy ECO_0000203 NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676732.RAMHv3Un88Lhpzo6WnnAwzazhX0W99Q0S73ERmA-hyZ_c130_provenance.