Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_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." NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_assertion evidence source_evidence_literature NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_assertion SIO_000772 11451544 NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_assertion wasDerivedFrom gad-20130706 NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_assertion wasGeneratedBy ECO_0000203 NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.
- gad-20130706 importedOn "2013-07-06" NP61321.RAsSUUBUKvjs_0gLWdEPQUhei_prfo1tlg3uBKwNzpw9g130_provenance.