Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_assertion description "[Molecular identification of hereditary persistence of fetal hemoglobin type 2 (HPFH type 2) in patients from Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_assertion evidence source_evidence_literature NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_assertion SIO_000772 7536477 NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_assertion wasDerivedFrom befree-20140225 NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_assertion wasGeneratedBy ECO_0000203 NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP748110.RAzgVb_T0uGWXO8B-IDQeqsVWS-ksYmYIyRT0ftHluvHw130_provenance.