Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_assertion description "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_assertion evidence source_evidence_literature NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_assertion SIO_000772 22946725 NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_assertion wasDerivedFrom befree-20150227 NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_assertion wasGeneratedBy ECO_0000203 NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP931093.RAwaXSI3Py6kJAvhhaS-mZrz3w1v6JacWJOsTkizPZRp0130_provenance.