Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_assertion description "[These results provide evidence of a significant role for genetic variation at the IFNG locus and provide detailed understanding of the genetic mechanisms underlying this association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_assertion evidence source_evidence_literature NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_assertion SIO_000772 16690980 NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_assertion wasDerivedFrom gad-20130706 NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_assertion wasGeneratedBy ECO_0000203 NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.
- gad-20130706 importedOn "2013-07-06" NP65137.RAIRwFe_BVMVC1bKGZzREcX0k0rFtJrtlkdO8YpDUkM7Q130_provenance.