Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_assertion description "[Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_assertion evidence source_evidence_literature NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_assertion SIO_000772 17367211 NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_assertion wasDerivedFrom befree-2016 NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_assertion wasGeneratedBy ECO_0000203 NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.
- befree-2016 importedOn "2016-02-19" NP599528.RAatJmV1uzj52Fn8Vg7PBAR0LTBN3p4lerBPZZpLDie2I130_provenance.