Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_assertion description "[Further studies are needed to explore contributions from other genetic factors such as rare variants in these genes and variation outside of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_assertion evidence source_evidence_literature NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_assertion SIO_000772 20810604 NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_assertion wasDerivedFrom gad-20130706 NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_assertion wasGeneratedBy ECO_0000203 NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52854.RAP4J0xsNXhIKt9Qg5EwSwwEny0JPjREJCr9vqrmY1kJk130_provenance.