Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_assertion description "[MTHFR gene mutation was evaluated in patients with severe pregnancy complications in northern Finland/mutation was homozygous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_assertion evidence source_evidence_literature NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_assertion SIO_000772 16514238 NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_assertion wasDerivedFrom lhgdn-20090331 NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_assertion wasGeneratedBy ECO_0000203 NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134317.RAqIM6xLAxirUd5_-zpH7xjzHxwSWN-9CbjMD1kvPttfM130_provenance.