Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_assertion description "[T102C polymorphism of the serotonin receptor 2A gene (5-HT2A) has been shown to be associated with certain diseases such as non-fatal acute myocardial infarction, essential hypertension, and alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_assertion evidence source_evidence_literature NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_assertion SIO_000772 17713649 NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_assertion wasDerivedFrom befree-20140225 NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_assertion wasGeneratedBy ECO_0000203 NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP604432.RAVuvIWCQVLggITvxkZgH1F2kxqMQBe-YLpyTMbvS4jq8130_provenance.