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- source_evidence_literature type ECO_0000212 NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_assertion description "[A significant association with CM was found for the long allele of monoamine oxidase A 30 bp VNTR and CYP1A2*1F variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_assertion evidence source_evidence_literature NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_assertion SIO_000772 20213484 NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_assertion wasDerivedFrom befree-2016 NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_assertion wasGeneratedBy ECO_0000203 NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.
- befree-2016 importedOn "2016-02-19" NP798646.RAG8OpE7CKRLKhU0BmHQUEwoAkC5MrPzEo-aui__bu56k130_provenance.