Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_assertion description "[We further analyzed mutations of the FANCC and FANCG genes, responsible for FA-C and FA-G, respectively, in the remaining 6 FA patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_assertion evidence source_evidence_literature NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_assertion SIO_000772 10807541 NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_assertion wasDerivedFrom befree-20140225 NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_assertion wasGeneratedBy ECO_0000203 NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP305650.RAEdOTwA5lMYiVVqME5ew-0KYNHL8QpB6R6QmwiqMPMIc130_provenance.