Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_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." NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_assertion evidence source_evidence_literature NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_assertion SIO_000772 14985373 NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_assertion wasDerivedFrom befree-2016 NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_assertion wasGeneratedBy ECO_0000203 NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.
- befree-2016 importedOn "2016-02-19" NP433137.RAavn-d5z1LJOdXuOX4SZoHC55lX8qQhpeHHaC399STfI130_provenance.