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- source_evidence_literature type ECO_0000212 NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_assertion description "[In conclusion, LRP gene polymorphisms, particularly the relatively common exon 22 C200T polymorphism, are a significant risk factor for premature CAD in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_assertion evidence source_evidence_literature NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_assertion SIO_000772 12732394 NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_assertion wasDerivedFrom befree-20150227 NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_assertion wasGeneratedBy ECO_0000203 NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP833203.RAXbKn9Kdgu3C7o1z8-h8U_XVakCwB5fw_wR6Vc6iKJgU130_provenance.