Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion> ?p ?o ?g. }
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- NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion type Assertion NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_head.
- NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion description "[C4 null alleles were significantly more common in Henoch-Schonlein purpura patients than in controls ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_provenance.
- NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion evidence source_evidence_literature NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_provenance.
- NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion SIO_000772 15787745 NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_provenance.
- NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion wasDerivedFrom lhgdn-20090331 NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_provenance.
- NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_assertion wasGeneratedBy ECO_0000203 NP209925.RAUkiAliE8OjEgsqMuBxWO_z4_9LX1t0R0xCD07btSHHc130_provenance.