Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.