Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_assertion description "[Therefore, possession of the SCNN1A G(2139) allele significantly increased the risk of hypertension. A lower level of SCNN1A subunit expression among subjects with the AA genotype might lead to lower levels of sodium reabsorption in the kidney and might p]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_assertion evidence source_evidence_literature NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_assertion SIO_000772 11752024 NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_assertion wasDerivedFrom gad-20150221 NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_assertion wasGeneratedBy ECO_0000203 NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72275.RAWlX4cm04JTlf0VpaTvihDDeJLji1Byi-cmBuScS09hU130_provenance.