Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_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." NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_assertion evidence source_evidence_literature NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_assertion SIO_000772 14985373 NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_assertion wasDerivedFrom befree-20140225 NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_assertion wasGeneratedBy ECO_0000203 NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP700372.RA1_71VJgnpQprYr6XwCWj4h_ecFkZhOOjXgx-z4IPezo130_provenance.