Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion description "[Haptoglobin polymorphism: a novel genetic risk factor for celiac disease development and its clinical manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion evidence source_evidence_literature NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion SIO_000772 18258668 NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion wasDerivedFrom befree-20150227 NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion wasGeneratedBy ECO_0000203 NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_provenance.