Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_assertion description "[We genotyped five polymorphisms of the AGT, ACE, AT1R, 5-HT2A, and 5-HTT genes in 245 patients with Hypertrophic Cardiomyopathy (HCM; 205 without an identified sarcomeric gene mutation), in 145 patients with LVH secondary to hypertension, and 300 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_assertion evidence source_evidence_literature NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_assertion SIO_000772 20594303 NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_assertion wasDerivedFrom befree-2016 NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_assertion wasGeneratedBy ECO_0000203 NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.
- befree-2016 importedOn "2016-02-19" NP822895.RAAl6d4LsHKWqU2SVU0zbGjPpMC2nvCAKyFhwfjjMRP1U130_provenance.