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- source_evidence_literature type ECO_0000212 NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion description "[To evaluate whether C3435T MDR1 polymorphism is associated with the occurrence and outcome of ALL, 113 children with ALL (median age 5.1 yr) and 175 healthy individuals of Polish Caucasian origin were studied by polymerase chain reaction-restriction fragment-length polymorphism (PCR-RFLP) assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion evidence source_evidence_literature NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion SIO_000772 15059065 NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion wasDerivedFrom befree-20140225 NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion wasGeneratedBy ECO_0000203 NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance.