Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_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." NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_assertion evidence source_evidence_literature NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_assertion SIO_000772 20400963 NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_assertion wasDerivedFrom befree-20140225 NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_assertion wasGeneratedBy ECO_0000203 NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.
- befree-20140225 importedOn "2014-02-25" NP821139.RAdVVuUK3Ki13H5KyArtTAXJmcaWhGKHQuqgeHFvBjS10130_provenance.