Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_assertion description "[Autosomal dominant familial spastic paraplegia (FSP) is a genetically heterogeneous neurodegenerative disorder displaying anticipation for which three loci have been mapped to the chromosomal positions 14q11.2-q24.3 (SPG3), 2p21-p24 (SPG4) and 15q11.1 (SPG6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_assertion evidence source_evidence_literature NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_assertion SIO_000772 9736780 NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_assertion wasDerivedFrom befree-20140225 NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_assertion wasGeneratedBy ECO_0000203 NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP524845.RAGYZfEybiVvbkgPlTt4Mm58GNK8N5RztQwHXOz1IQRnI130_provenance.