Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_assertion description "[It encompasses a spectrum of disorders including multiple endocrine neoplasia types 1 (MEN1) and 2A, hyperparathyroidism-jaw tumour syndrome (HPT-JT), familial hypocalciuric hypercalcaemia (FHH), and familial isolated hyperparathyroidism (FIHP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_assertion evidence source_evidence_literature NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_assertion SIO_000772 14985373 NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_assertion wasDerivedFrom befree-20150227 NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_assertion wasGeneratedBy ECO_0000203 NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP553569.RAVrm-Oi19Jb7sffHQWKO08ajwN_E5Kby1HYtEqlntxtA130_provenance.