Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_assertion description "[Using genome-wide association methodology, we have successfully identified a SNP in complete LD with a sequence variant previously shown to be strongly associated with factor VII, providing proof of principle for this approach. Further study of additional]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_assertion evidence source_evidence_literature NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_assertion SIO_000772 17903294 NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_assertion wasDerivedFrom gad-20150221 NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_assertion wasGeneratedBy ECO_0000203 NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP112593.RAlvmPKI2_EeA_5QjcQ6Xqz5f_r6IBntEyISZ4qFEurLU130_provenance.