Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_assertion description "[FRAXA (FMR1) trinucleotide expansion is widely searched in routine screening, but found in only about 2% of the patients tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_assertion evidence source_evidence_literature NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_assertion SIO_000772 17383248 NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_assertion wasDerivedFrom befree-20150227 NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_assertion wasGeneratedBy ECO_0000203 NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409018.RAc7p_EyE_I0u0lYOpCDQfit4wyiIwjXabktkqn9Cntrs130_provenance.