Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_assertion wasGeneratedBy ECO_0000203 NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_assertion wasDerivedFrom befree-2016 NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_assertion SIO_000772 15661754 NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_assertion evidence source_evidence_literature NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.
- NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_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." NP477150.RAOfNiYqOcXORss8cR71oM4gvcp4B3mYN_DLmv8gN5o6Y130_provenance.