Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion description "[Loss of function of paraplegin (encoded by the SPG7 gene) causes hereditary spastic paraplegia, a disease characterized by retrograde degeneration of cortical motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion evidence source_evidence_literature NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion SIO_000772 19289403 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion wasDerivedFrom befree-20140225 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion wasGeneratedBy ECO_0000203 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.