Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_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." NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_assertion evidence source_evidence_literature NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_assertion SIO_000772 8341140 NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_assertion wasDerivedFrom befree-20150227 NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_assertion wasGeneratedBy ECO_0000203 NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.
- befree-20150227 importedOn "2015-02-27" NP275836.RAyZWLCRJMOWuW8hcXRC7-6smp2ppFZGFkK6niP42Q0ww130_provenance.