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- source_evidence_literature type ECO_0000212 NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_assertion description "[We conclude that the presence of 1 or 2 C4A null allotypes and the presence of a C4A gene deletion identify subgroups of patients with SLE that differ in clinical, laboratory, and autoantibody characteristics from other patients with SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_assertion evidence source_evidence_literature NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_assertion SIO_000772 8341140 NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_assertion wasDerivedFrom befree-2016 NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_assertion wasGeneratedBy ECO_0000203 NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1339162.RAwICCM3gW0ZmCVUu7Qy9e9GcWCob58m1T208_vJPZnzw130_provenance.