Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_assertion description "[Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_assertion evidence source_evidence_curated NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_assertion SIO_000772 14583443 NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_assertion wasDerivedFrom uniprot-2016 NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_assertion wasGeneratedBy ECO_0000218 NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3071.RAd_EPd9h5GaO1MnbjkfEPwEUaKnGfhqKS1YuICPrckps130_provenance.