Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_assertion description "[The aim of the study was to investigate the association between the common variants of apelin gene (APLN) and hypertension, which was reported recently in a Chinese Han population with and without diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_assertion evidence source_evidence_literature NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_assertion SIO_000772 23316219 NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_assertion wasDerivedFrom befree-2016 NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_assertion wasGeneratedBy ECO_0000203 NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.
- befree-2016 importedOn "2016-02-19" NP1043385.RAoF2ZFLmhOE8J8OBV-NGSFQM0QNpSU76NcpxO5VfJLow130_provenance.