Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_assertion evidence source_evidence_literature NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_assertion SIO_000772 17646629 NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_assertion wasDerivedFrom lhgdn-20090331 NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_assertion wasGeneratedBy ECO_0000203 NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.