Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_assertion description "[All mutations of atlastin1 in young-onset autosomal dominant spastic paraplegia patients in France were found in exons 7, 8, 12, and 13/exons should be given priority when performing molecular diagnoses for SPG3A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_assertion evidence source_evidence_literature NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_assertion SIO_000772 15596607 NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_assertion wasDerivedFrom lhgdn-20090331 NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_assertion wasGeneratedBy ECO_0000203 NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP153438.RAhG2GY8nI-lkJ7uKIdGNFu7nmkrqq51RuhfZ1SrzqjOg130_provenance.