Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_assertion wasGeneratedBy ECO_0000203 NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_assertion wasDerivedFrom befree-20140225 NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_assertion SIO_000772 15661754 NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_assertion evidence source_evidence_literature NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_assertion description "[Both the total number of chromosome gaps and breaks and breaks at the specific common fragile sites FRA3B and FRA16D were significantly elevated in the absence of an intact FA pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743359.RAJUTFfHAcaoopFtoqLOn6hwZ1RleDj0MXAjT1gJS6n_k130_provenance.