Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_assertion description "[A novel single-nucleotide polymorphism (SNP), 829C-->T in the 3'-untranslated region of the human dihydrofolate reductase (DHFR) gene transcript, was identified in the study population of 37 patients with childhood leukemias/lymphomas and 83 healthy Japanese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_assertion evidence source_evidence_literature NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_assertion SIO_000772 11448909 NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_assertion wasDerivedFrom befree-20140225 NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_assertion wasGeneratedBy ECO_0000203 NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP695764.RAGWG1CTI-oRksCApSruI549Q84E9vVM4M1TNRCzRnptU130_provenance.