Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_assertion description "[These findings suggest that in Japanese individuals, this deletion in the human NP receptor gene reduces receptor activity and may confer increased susceptibility to developing EH or left ventricular hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_assertion evidence source_evidence_literature NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_assertion SIO_000772 10785505 NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_assertion wasDerivedFrom befree-2016 NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_assertion wasGeneratedBy ECO_0000203 NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.
- befree-2016 importedOn "2016-02-19" NP282504.RAeTAnmGwmpx45CPTFXai1iXYod5aei4lzBcNPhGeBdq4130_provenance.