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- source_evidence_literature type ECO_0000212 NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_assertion description "[The aim of the present study was to explore whether genetic variations of ET-1 (G/T substitution that predicts an Lys/Asn change at codon 198) and its receptor ET(A) (T/C in exon 6, H323H) could predispose carriers to heart failure (HF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_assertion evidence source_evidence_literature NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_assertion SIO_000772 16582543 NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_assertion wasDerivedFrom befree-20140225 NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_assertion wasGeneratedBy ECO_0000203 NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP726390.RAoIu0h0LZ1KFMI-TFA-kIiT1NJXRtkT0zvKCREKd7R4E130_provenance.