Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_assertion description "[Mutations in the CFH gene are associated with atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis type II and C3 glomerulonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_assertion evidence source_evidence_literature NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_assertion SIO_000772 21270828 NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_assertion wasDerivedFrom befree-2016 NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_assertion wasGeneratedBy ECO_0000203 NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.
- befree-2016 importedOn "2016-02-19" NP868118.RAlcH67yybbQ-rqT637IOaf-JTDaZB79dcH4fKFwWeXmw130_provenance.