Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- befree-2016 importedOn "2016-02-19" NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_assertion wasGeneratedBy ECO_0000203 NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_assertion wasDerivedFrom befree-2016 NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_assertion SIO_000772 18372405 NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_assertion evidence source_evidence_literature NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.
- NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_assertion description "[Mutation analysis and characterization of HSD17B2 sequence variants in breast cancer cases from French Canadian families with high risk of breast and ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662733.RAyM2E1y9zM9xRpCYc9tMBz6IN5F1WzRnYPEhqrUUv_e4130_provenance.