Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_assertion description "[We provide evidence of increased risk in subjects with the GGMT variant of associated genotype of AGT gene for CHF, especially of fifteen-fold risk of this variant in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_assertion evidence source_evidence_literature NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_assertion SIO_000772 12767551 NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_assertion wasDerivedFrom befree-2016 NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_assertion wasGeneratedBy ECO_0000203 NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.
- befree-2016 importedOn "2016-02-19" NP395749.RAi8_QV6QOYOysA-S0hDfXh0j2OGB79jP9247RwHMykF0130_provenance.