Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion wasGeneratedBy ECO_0000203 NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion wasDerivedFrom befree-20140225 NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion SIO_000772 15661754 NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion evidence source_evidence_literature NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_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." NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance.