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- source_evidence_literature type ECO_0000212 NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_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." NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_assertion evidence source_evidence_literature NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_assertion SIO_000772 20400963 NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_assertion wasDerivedFrom befree-20150227 NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_assertion wasGeneratedBy ECO_0000203 NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663574.RAb-2ltqlcYjcpyitcJgPIt3eoexKNHKalcX51GHnEbfU130_provenance.