Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_assertion evidence source_evidence_literature NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_assertion SIO_000772 18714162 NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_assertion wasDerivedFrom befree-20140225 NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_assertion wasGeneratedBy ECO_0000203 NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455003.RA9jvBoK0LbCAoNmMbo-MfXkzaqOkxJJ8HaarGN23S_Cs130_provenance.