Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_assertion description "[Genotypes that cause disease at the phenylalanine hydroxylase (PAH) gene and galactose-1-phosphate uridyltransferase (GALT) gene in a group of 101 hyperphenylalaninaemic and 77 patients with classic galactosaemia were established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_assertion evidence source_evidence_literature NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_assertion SIO_000772 11678552 NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_assertion wasDerivedFrom gad-20150221 NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_assertion wasGeneratedBy ECO_0000203 NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP51708.RAxeL4_oNPoaGPW2EGxWZN4jt8HJyhKIZEsKaiZA1_Cyg130_provenance.