Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_assertion description "[To investigate this point, we compared the mutant levels in 51 first polar bodies (PBs) and their counterpart (oocytes, blastomeres, or whole embryos), at risk of having (1) the `MELAS` m.3243A>G mutation in MT-TL1 (n = 30), (2) the `MERRF` m.8344A>G mutation in MT-TK (n = 15), and (3) the m.9185T>G mutation located in MT-ATP6 (n = 6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_assertion evidence source_evidence_literature NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_assertion SIO_000772 21473984 NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_assertion wasDerivedFrom befree-20140225 NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_assertion wasGeneratedBy ECO_0000203 NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.
- befree-20140225 importedOn "2014-02-25" NP695836.RADp92G5YZdqqNCkTPiegI8KDTDxcPHpJTWrJsBb8GH24130_provenance.