Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_assertion description "[Systematic screening using the SSCP technique followed by sequencing of bands with abnormal mobility derived from the AGXT exons of 15 unrelated Italian patients with primary hyperoxaluria type 1 (PH1) allowed us to characterize both the mutant alleles in each individual.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_assertion evidence source_evidence_curated NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_assertion SIO_000772 10453743 NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_assertion wasDerivedFrom uniprot-20150221 NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_assertion wasGeneratedBy ECO_0000218 NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1886.RApH9hk758TQVSK9xDcUyN-8w4rCFEWkZt081_x-HhbeE130_provenance.