Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion wasGeneratedBy ECO_0000203 NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion wasDerivedFrom befree-20140225 NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion SIO_000772 17914928 NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion evidence source_evidence_literature NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.