Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_assertion wasGeneratedBy ECO_0000203 NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_assertion wasDerivedFrom befree-20140225 NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_assertion SIO_000772 10097123 NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_assertion evidence source_evidence_literature NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_assertion description "[Subsequently, one was identified as Gnas, which encodes a G protein alpha subunit, and there is clinical and biochemical evidence that the human homologue GNAS1, mutated in patients with Albright hereditary osteodystrophy, is also imprinted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP207656.RAKW4puuApw5CxlLGyZeyDLFJh-jaMZxXlmCnkSUKQ0oA130_provenance.