Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_assertion description "[NOD2 genotyping may help predict disease progression in patients with Blau syndrome/EOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_assertion evidence source_evidence_literature NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_assertion SIO_000772 19116920 NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_assertion wasDerivedFrom befree-20150227 NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_assertion wasGeneratedBy ECO_0000203 NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP937811.RAOHW5hkqI1ZuEHIClGxsOUCzH5bBJ4sdL3iVwR4pjH_w130_provenance.