Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_assertion description "[X-linked hypophosphatemic rickets/osteomalacia (XLH), autosomal dominant and recessive hypophosphatemic rickets/osteomalacia (ADHR and ARHR) share common clinical features including high fibroblast growth factor 23 (FGF23) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_assertion evidence source_evidence_literature NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_assertion SIO_000772 19581284 NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_assertion wasDerivedFrom befree-20150227 NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_assertion wasGeneratedBy ECO_0000203 NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355841.RAqn9ZvQDT9m_CC9gU9vBXBRQ7x4ry_1NFHhsP4PIFsSI130_provenance.