Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_assertion description "[Families carrying ACD and TERF2IP mutations were also enriched with other cancer types, suggesting that these variants also predispose to a broader spectrum of cancers than just melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_assertion evidence source_evidence_literature NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_assertion SIO_000772 25505254 NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_assertion wasDerivedFrom befree-2016 NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_assertion wasGeneratedBy ECO_0000203 NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248148.RA9HFrWGejvC7GJMqy4fN6mqNzGeNt1IDp16yODx9qL_g130_provenance.