Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_assertion description "[Tyrosinemia type II (Richner-Hanhart syndrome, RHS) is a disorder of autosomal recessive inheritance characterized by keratitis, palmoplantar hyperkeratosis, mental retardation, and elevated blood tyrosine levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_assertion evidence source_evidence_literature NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_assertion SIO_000772 9544843 NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_assertion wasDerivedFrom befree-20140225 NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_assertion wasGeneratedBy ECO_0000203 NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789482.RAuGugZHfcPoh_QnMDu0c0ZRKbsHEQxQ-nqFCXDZZoWyA130_provenance.