Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_assertion description "[ Combined heterozygosity for MTHFR mutations C677T and A1298C may represent a genetic marker for abruptio placentae.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_assertion evidence source_evidence_literature NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_assertion SIO_000772 11451544 NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_assertion wasDerivedFrom gad-20150221 NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_assertion wasGeneratedBy ECO_0000203 NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP70704.RAeczHNNgnpDGgzqEDoqq09VNBrE0ZUVYtUr2kxJR36gs130_provenance.