Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_assertion description "[ Our data show that the K1019X mutation in the EphB2 gene differs in frequency between AA and EA, is associated with increased risk for PC in AA men with a positive family history, and may be an important genetic risk factor for prostate cancer in AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_assertion evidence source_evidence_literature NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_assertion SIO_000772 16155194 NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_assertion wasDerivedFrom gad-20130706 NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_assertion wasGeneratedBy ECO_0000203 NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.
- gad-20130706 importedOn "2013-07-06" NP45091.RAAqkSQsWtWAPM12uU7QEwe-91hGl4XCDyMt9OpqFYj7E130_provenance.