Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_assertion description "[We report here a series of six patients with severe CTP deficiency, four males and two females; clinical presentations include mild to severe mental retardation (6/6), associated with psychiatric symptoms (5/6: autistic behaviour, chronic hallucinatory psychosis), seizures (2/6) and muscular symptoms (2/4 males).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_assertion evidence source_evidence_literature NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_assertion SIO_000772 21660517 NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_assertion wasDerivedFrom befree-20140225 NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_assertion wasGeneratedBy ECO_0000203 NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP639681.RAxo2CK0-SYFhdKE9PDlCHqOuA_sSRIlW0-ImFoDVqhLs130_provenance.