Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion evidence source_evidence_literature NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion SIO_000772 20857310 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion wasDerivedFrom befree-20140225 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion wasGeneratedBy ECO_0000203 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.