Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_assertion description "[Using FISH with a panel of 11q and 21q cosmid/YAC probes, we localized the chromosome 11 breakpoint at q23.3 in a region flanked by CP-921G9 and CP-939H3 YACs, distal to the HRX/MLL locus frequently involved in acute leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_assertion evidence source_evidence_literature NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_assertion SIO_000772 10451699 NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_assertion wasDerivedFrom befree-20140225 NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_assertion wasGeneratedBy ECO_0000203 NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP302018.RAhbfXkzq4SUaLY5tGWM4mpW9dmjydVyLvrd7vDbl87Mg130_provenance.