Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_assertion description "[Maternally derived mutations are usually associated with resistance to parathyroid hormone termed pseudohypoparathyroidism type Ia. Paternally derived mutations are associated with AHO but usually normal hormone responsiveness, known as pseudo-pseudohypoparathyroidism. These observations can be explained by tissue-specific GNAS1 imprinting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_assertion evidence source_evidence_literature NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_assertion SIO_000772 12624854 NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_assertion wasDerivedFrom befree-2016 NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_assertion wasGeneratedBy ECO_0000203 NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.
- befree-2016 importedOn "2016-02-19" NP386250.RAGDh4AS8_i9gch71QeKtYKUejXv0FyV2dMjC7ugooBwA130_provenance.