Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_assertion description "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_assertion evidence source_evidence_literature NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_assertion SIO_000772 10667475 NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_assertion wasDerivedFrom befree-20140225 NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_assertion wasGeneratedBy ECO_0000203 NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.