Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_assertion type Assertion NP463514.RAqmS8TRF_Z4uChwV4zdD9EtvFOirEBULdXNNr9YFBppA130_head.
- 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.