Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion> ?p ?o ?g. }
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- NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion type Assertion NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_head.
- NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion description "[Selected exonic sequencing of the AGXT gene provides a genetic diagnosis in 50% of patients with primary hyperoxaluria type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_provenance.
- NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion evidence source_evidence_curated NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_provenance.
- NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion SIO_000772 17495019 NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_provenance.
- NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion wasDerivedFrom uniprot-2016 NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_provenance.
- NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_assertion wasGeneratedBy ECO_0000218 NP4981.RARIec_qRRqNSNNzYlxQ_IbiAYZr74cr60JhKLtXhAnQQ130_provenance.