Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_assertion wasGeneratedBy ECO_0000203 NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_assertion wasDerivedFrom befree-20140225 NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_assertion SIO_000772 21872273 NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_assertion evidence source_evidence_literature NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_assertion description "[Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive disorder characterized by ichthyosis, spastic di- or tetraplegia and mental retardation due a defect of the fatty aldehyde dehydrogenase (FALDH), related to mutations in the ALDH3A2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP431072.RADWP5YiLm-2tvY-LGA9VozZFWJPYII-5glBdGwTUshAM130_provenance.