Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_assertion description "[Novel mutations in ABCA1 gene in Japanese patients with Tangier disease and familial high density lipoprotein deficiency with coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_assertion evidence source_evidence_literature NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_assertion SIO_000772 11476965 NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_assertion wasDerivedFrom befree-2016 NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_assertion wasGeneratedBy ECO_0000203 NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.
- befree-2016 importedOn "2016-02-19" NP325276.RADvIqPovj13Kj0TDy7PJTMLy5NNi92LDClEXy9tPgYO4130_provenance.