Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_assertion description "[Affected cellular pathways may be modulated in sporadic malignancies and silencing of FANCF through methylation has been shown to cause somatic disruption of the FA pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_assertion evidence source_evidence_literature NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_assertion SIO_000772 16803569 NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_assertion wasDerivedFrom befree-2016 NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_assertion wasGeneratedBy ECO_0000203 NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.
- befree-2016 importedOn "2016-02-19" NP556755.RAEFtLdIVAwSN8Eyo4uW_54WWK-_J5KOoeY6utbRp1YtU130_provenance.