Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_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." NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_assertion evidence source_evidence_literature NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_assertion SIO_000772 11804203 NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_assertion wasDerivedFrom gad-20150221 NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_assertion wasGeneratedBy ECO_0000203 NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72689.RAGIt9wGcaEaSsif0uJm5PLdwqDpUSQ4VdKnwKpVsQfls130_provenance.