Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion> ?p ?o ?g. }
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- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion type Assertion NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_head.
- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion evidence source_evidence_literature NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion SIO_000772 22236406 NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion wasDerivedFrom befree-20140225 NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion wasGeneratedBy ECO_0000203 NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.