Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_assertion description "[The SDF-1 homozygous 3'A variant was related to more-rapid disease progression, and CCR5 Delta32 was associated with reduced rates of hazard for disease progression in nucleoside-treated subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_assertion evidence source_evidence_literature NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_assertion SIO_000772 11709782 NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_assertion wasDerivedFrom gad-20130706 NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_assertion wasGeneratedBy ECO_0000203 NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP46372.RANDz3zj-tpOJ8sxJv3BjT0PgNOTa89kW7CT9TN-_FWYM130_provenance.