Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_assertion description "[We hypothesized that the EGF A61G homozygous variant genotype (GG) is (a) both a risk and poor prognostic factor for EAC and (b) associated with higher EGF serum levels in individuals with gastroesophageal reflux disease (GERD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_assertion evidence source_evidence_literature NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_assertion SIO_000772 18483390 NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_assertion wasDerivedFrom befree-20140225 NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_assertion wasGeneratedBy ECO_0000203 NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP716153.RA70-qquaxZlOJyhvq7p4X4Z0oL2s6_MShSpsJut2EZpI130_provenance.