Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_assertion description "[16 patients from 11 unrelated families were studied with a phenotype of infantile ascending hereditary spastic paralysis (IAHSP); Alsin mutations were found in 4 of the 10 families, whereas haplotype analysis excluded the ALS2 locus in one family ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_assertion evidence source_evidence_literature NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_assertion SIO_000772 12601111 NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_assertion wasDerivedFrom lhgdn-20090331 NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_assertion wasGeneratedBy ECO_0000203 NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP216667.RAj8koxet72E3cr-dTsSymPKnrPff8pis2u1JA7XNtEsY130_provenance.