Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- befree-2016 importedOn "2016-02-19" NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_assertion wasGeneratedBy ECO_0000203 NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_assertion wasDerivedFrom befree-2016 NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_assertion SIO_000772 18055909 NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_assertion evidence source_evidence_literature NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.
- NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_assertion description "[These data suggest that non-synonymous GATA4 sequence variants are found in a small percentage of patients with septal defects and are very uncommonly found in patients with conotruncal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643121.RAibs5iAtauuGjz9gTvijt28slA69fSPlW3UTM54tOQDk130_provenance.