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- source_evidence_literature type ECO_0000212 NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_assertion description "[For one locus containing CD2, we found that a missense variant, rs699738 (c.798C>A [p.His266Gln]), and a noncoding variant, rs624988, reside on distinct haplotypes and independently contribute to the risk of RA (p = 4.6 � 10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_assertion evidence source_evidence_literature NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_assertion SIO_000772 23261300 NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_assertion wasDerivedFrom befree-20140225 NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_assertion wasGeneratedBy ECO_0000203 NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP522467.RA6pAE9wWCpqdMBt3ni4ocRGUsqyS4f9ekGISmiIpycuA130_provenance.