Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_assertion description "[We have previously characterized mutant adenosine deaminase (ADA; adenosine aminohydrolase, EC 3.5.4.4) enzymes in seven children with partial ADA deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_assertion evidence source_evidence_literature NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_assertion SIO_000772 2166947 NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_assertion wasDerivedFrom befree-2016 NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_assertion wasGeneratedBy ECO_0000203 NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.
- befree-2016 importedOn "2016-02-19" NP901587.RA_wJUSLFfZvTy4DjuCNUgSeQc5ZuH6kloXVwa_L9bA9I130_provenance.