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- source_evidence_literature type ECO_0000212 NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_assertion description "[Across RXRA, one haplotype located 3' of the coding sequence (rs748964, rs3118523), increased RCC risk 35% among individuals with the variant haplotype compared to those with the most common haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_assertion evidence source_evidence_literature NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_assertion SIO_000772 19753122 NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_assertion wasDerivedFrom befree-2016 NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_assertion wasGeneratedBy ECO_0000203 NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.
- befree-2016 importedOn "2016-02-19" NP763125.RA0ODBaGP_GY8xFOgByPltdNd3fnmklxY7MKg9wrdvMg4130_provenance.