Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_assertion description "[XRCC1 and XRCC3 variants and risk of glioma and meningioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_assertion evidence source_evidence_literature NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_assertion SIO_000772 18330515 NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_assertion wasDerivedFrom befree-20150227 NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_assertion wasGeneratedBy ECO_0000203 NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP780620.RALTfX5gH59oFm3R6LAFhKvDWK4EDqoW9tPogO_z5xvXw130_provenance.