Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_assertion description "[This study emphasizes that modifiers such as CD46 and FHL-1 may determine the kidney phenotype of patients who present with homozygous CFH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_assertion evidence source_evidence_literature NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_assertion SIO_000772 23870792 NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_assertion wasDerivedFrom befree-2016 NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_assertion wasGeneratedBy ECO_0000203 NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.
- befree-2016 importedOn "2016-02-19" NP1095241.RA1Uws_uplJMA4qTycB0CyrJhYZ1Rmev2tAETl2EzQ1go130_provenance.