Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_assertion description "[IDH mutations in gliomas are associated with several clinically relevant parameters including patient age, histopathological diagnosis, combined 1p/19q deletion, TP53 mutation, MGMT promoter hypermethylation and patient survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_assertion evidence source_evidence_literature NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_assertion SIO_000772 21955925 NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_assertion wasDerivedFrom befree-20140225 NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_assertion wasGeneratedBy ECO_0000203 NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241578.RAVtXInNQJl89E2ZKUnb7xfWkvAZgxYlwAIhCKbgq16jU130_provenance.