Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_assertion description "[A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_assertion evidence source_evidence_literature NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_assertion SIO_000772 15042429 NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_assertion wasDerivedFrom befree-2016 NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_assertion wasGeneratedBy ECO_0000203 NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.
- befree-2016 importedOn "2016-02-19" NP437011.RA-vp4MhVzqlSHgtNDyVgkjfsaphadgUTe_FGTo85ul8w130_provenance.