Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_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." NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_assertion evidence source_evidence_literature NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_assertion SIO_000772 21660517 NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_assertion wasDerivedFrom befree-2016 NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_assertion wasGeneratedBy ECO_0000203 NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.
- befree-2016 importedOn "2016-02-19" NP900911.RAlSSPBvUgiqkE5J07wHWAWa3lwhIOPB5GzYnmdvEMaW8130_provenance.