Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_assertion description "[Carbohydrate-deficient glycoprotein syndrome type 1 (CDG1) (MIM: 212065) is an autosomal recessive disorder with psychomotor retardation, strokelike episodes, ataxia, and olivopontocerebellar atrophy (OPCA) of neonatal onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_assertion evidence source_evidence_literature NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_assertion SIO_000772 10066032 NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_assertion wasDerivedFrom befree-2016 NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_assertion wasGeneratedBy ECO_0000203 NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.
- befree-2016 importedOn "2016-02-19" NP246959.RAO_9Pg3J2Bq7vOqoi027tXKI4crkIyljAOVFbHdVtpks130_provenance.