Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_assertion description "[There are two known disorders of creatine synthesis (both transmitted as autosomal recessive traits: arginine: glycine amidinotransferase (AGAT) deficiency; OMIM 602360; and guanidinoacetate methyltransferase (GAMT) deficiency (OMIM 601240)) and one disorder of creatine transport (X-linked recessive SLC6A8 creatine transporter deficiency (OMIM 300036)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_assertion evidence source_evidence_literature NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_assertion SIO_000772 21308988 NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_assertion wasDerivedFrom befree-20140225 NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_assertion wasGeneratedBy ECO_0000203 NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP266499.RAjCH1dnMtZMMwonI-qeIh-B1jsqAYR-95LY-9zc68FbQ130_provenance.