Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_assertion description "[Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_assertion evidence source_evidence_literature NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_assertion SIO_000772 19309693 NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_assertion wasDerivedFrom befree-20140225 NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_assertion wasGeneratedBy ECO_0000203 NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP626278.RA3aWbhJR9H9VwHMqQcEtWF8my9vV8rQMnkPxnLvef3-o130_provenance.