Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_assertion description "[AIP variants were detected in 3% of the 127 patients, comprising four of 48 patients with acromegaly (8%), 0 of 43 with prolactinomas, 0 of the 20 patients with non-functioning adenomas, 0 of 15 with corticotroph adenomas and 0 of one with a thyrotroph adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_assertion evidence source_evidence_literature NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_assertion SIO_000772 25184284 NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_assertion wasDerivedFrom befree-20150227 NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_assertion wasGeneratedBy ECO_0000203 NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP915916.RAbGZ6VLgQTvap1beo2jWvHpiIuh5Qe1FeyTjSU82nt8U130_provenance.