Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_assertion description "[Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_assertion evidence source_evidence_literature NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_assertion SIO_000772 15735798 NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_assertion wasDerivedFrom befree-2016 NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_assertion wasGeneratedBy ECO_0000203 NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.
- befree-2016 importedOn "2016-02-19" NP482948.RAiiGoc78sSt9TDpECYZxGdhnv8nGyg_nAMGt4i_J1zUE130_provenance.