Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_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." NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion evidence source_evidence_literature NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion SIO_000772 17646629 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion wasDerivedFrom lhgdn-20090331 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_assertion wasGeneratedBy ECO_0000203 NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_provenance.