Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- befree-2016 importedOn "2016-02-19" NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_assertion wasGeneratedBy ECO_0000203 NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_assertion wasDerivedFrom befree-2016 NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_assertion SIO_000772 14681881 NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_assertion evidence source_evidence_literature NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.
- NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_assertion description "[Our aim was to review the clinical features of 29 infants affected with SMARD1 and report on 26 novel IGHMBP2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425156.RAwT2WqroEzXr73_Q7IX0D5gHnKBOpQim9l8l0G-hX7u8130_provenance.