Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_assertion description "[We observed three alleles, A (AC)16, B (AC)14, and C (AC)18, with a frequency of between 68.2% and 86.9%, 13.1% and 18.2%, and 6.7% and 13.7%, respectively. Allele C was present only in Purepecha and Mestizo groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_assertion evidence source_evidence_literature NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_assertion SIO_000772 11804203 NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_assertion wasDerivedFrom gad-20130706 NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_assertion wasGeneratedBy ECO_0000203 NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP42675.RADEF_y6xY72XSf7MCxkoUQmBuPD1NcpEZUXu2uA1rmX0130_provenance.