Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion type Assertion NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_head.
- NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion description "[Familial defective apolipoprotein B-100 (FDB) is a genetic disorder caused by a substitution of glutamine for arginine at residue 3500 of the apolipoprotein B-100 molecule.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion evidence source_evidence_literature NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion SIO_000772 10984082 NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion wasDerivedFrom befree-20150227 NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_assertion wasGeneratedBy ECO_0000203 NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.