Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_assertion description "[Conversely, congenital heart defects, particularly mitral valve and septal defects, and ocular anomalies seem to be less frequent among MEK1/MEK2 mutation-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_assertion evidence source_evidence_literature NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_assertion SIO_000772 19156172 NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_assertion wasDerivedFrom gad-20150221 NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_assertion wasGeneratedBy ECO_0000203 NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP139296.RA07jcyDWaWMWgH9_68gKjJCas5QkkZiIoIebx5X8-ja8130_provenance.