Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion type Assertion NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_head.
- NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion description "[Genetic defects in human pericentrin (PCNT), encoding the centrosomal protein pericentrin, cause a form of osteodysplastic primordial dwarfism that is sometimes reported to be associated with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_provenance.
- NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion evidence source_evidence_literature NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_provenance.
- NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion SIO_000772 21270239 NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_provenance.
- NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion wasDerivedFrom befree-2016 NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_provenance.
- NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_assertion wasGeneratedBy ECO_0000203 NP868022.RAZUXYx7ztYzExT7W_YrP51Gbp0H0gFKnh51iahWJ_F5A130_provenance.