Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_assertion wasGeneratedBy ECO_0000203 NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_assertion wasDerivedFrom befree-20140225 NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_assertion SIO_000772 18079167 NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_assertion evidence source_evidence_literature NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_assertion description "[The mutation frequency varied according to the phenotype, from 41%, in HSP patients presenting with a thin corpus callosum (TCC) visualized by MRI, to 4.5%, in patients with mental impairment without a TCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP558940.RAbVL-VjcPp1xtP2bjUQCT-Ey--S5IepEiuyZYXx8LvAU130_provenance.