Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP243863.RAAD46HpHKXjM6SBy5IcVtMTp5P0i1UL7k6N6mZB5fiMg130_provenance.