Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_assertion wasGeneratedBy ECO_0000203 NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_assertion wasDerivedFrom befree-20150227 NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_assertion SIO_000772 15661754 NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_assertion evidence source_evidence_literature NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.
- NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_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." NP907938.RA8vA-4gVthD8bLs6CAU80gSois7_rRPjABrBe7cWtzV8130_provenance.