Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_assertion description "[A database has been created to collect information on families carrying a germ-line mutation in the TP53 gene and on families affected with Li-Fraumeni syndromes [Li-Fraumeni syndrome (LFS) and Li-Fraumeni-like syndrome (LFL)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_assertion evidence source_evidence_literature NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_assertion SIO_000772 14583457 NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_assertion wasDerivedFrom befree-20150227 NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_assertion wasGeneratedBy ECO_0000203 NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.
- befree-20150227 importedOn "2015-02-27" NP754856.RAAz3O8ASnV8CCGlXidm4TnUgclP72H69VLyA2KMSjV78130_provenance.