Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_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." NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_assertion evidence source_evidence_curated NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_assertion SIO_000772 12624854 NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_assertion wasDerivedFrom uniprot-20130724 NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_assertion wasGeneratedBy ECO_0000218 NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2824.RAMTS4CcLLaSFx0ZaOnZLStN8X4ufUQIXGqfSxEgANkho130_provenance.