Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_assertion description "[In a nested case-control study, we evaluated 98 single-nucleotide polymorphisms (SNPs) in 17 RGS genes for the risk of SPT/recurrence among 450 HNSCC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_assertion evidence source_evidence_literature NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_assertion SIO_000772 20627871 NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_assertion wasDerivedFrom befree-20140225 NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_assertion wasGeneratedBy ECO_0000203 NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP330162.RA6dU_CpKJWQa6joReG5G3yQlqzBMe9BcpyR3mn833ia0130_provenance.