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- source_evidence_literature type ECO_0000212 NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_assertion description "[Thus, biallelic germline mutations in a RAD51 paralog are associated with an FA-like syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_assertion evidence source_evidence_literature NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_assertion SIO_000772 20400963 NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_assertion wasDerivedFrom befree-2016 NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_assertion wasGeneratedBy ECO_0000203 NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP806791.RAnL2la2U_F9lb3OQeR7eHlYc1JQZa22ImLV1d-e6O05Y130_provenance.