Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion> ?p ?o ?g. }
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- NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion type Assertion NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_head.
- NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion description "[Analysis of GNAS1 and overlapping transcripts identifies the parental origin of mutations in patients with sporadic Albright hereditary osteodystrophy and reveals a model system in which to observe the effects of splicing mutations on translated and untranslated messenger RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_provenance.
- NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion evidence source_evidence_literature NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_provenance.
- NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion SIO_000772 12624854 NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_provenance.
- NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion wasDerivedFrom befree-2016 NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_provenance.
- NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_assertion wasGeneratedBy ECO_0000203 NP386247.RAcEW9w2DPS-GYKY03h5MV4-B2vO42GIEoOiqOsXPZS9A130_provenance.