Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_assertion description "[A substantial portion of remaining patients have mutations of the genes encoding cartilage oligomeric matrix protein or diastrophic dysplasia sulfate transporter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_assertion evidence source_evidence_literature NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_assertion SIO_000772 8879993 NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_assertion wasDerivedFrom befree-20140225 NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_assertion wasGeneratedBy ECO_0000203 NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.
- befree-20140225 importedOn "2014-02-25" NP332280.RAPXNbLXhsdX3p5EN0WDb1kE2VtyR-KkHsy7lVed2n_60130_provenance.