Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_assertion wasGeneratedBy ECO_0000203 NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_assertion wasDerivedFrom befree-20140225 NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_assertion SIO_000772 18425437 NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_assertion evidence source_evidence_literature NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_assertion description "[Deficiency of dihydropteridine reductase causes a variant form of phenylketonuria associated with a devastating neurological disease characterized by mental retardation, hypokinesis and other features relating to basal ganglia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589758.RAGtlFbZXjNjqj4_00pdOhGEX6ir46I2pdPA9sSdJWxj4130_provenance.