Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_assertion description "[It is not clear whether this association derives from immune dysfunction related to the absent isotype or from another disease susceptibility gene closely linked to C4B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_assertion evidence source_evidence_literature NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_assertion SIO_000772 2573592 NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_assertion wasDerivedFrom befree-20140225 NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_assertion wasGeneratedBy ECO_0000203 NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP438982.RAU8gJLDQgIfNv3EVEaDIhkleRVeTksf5Vcz9qckF3AVc130_provenance.