Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_assertion description "[Complete deficiencies of complement components C4A and C4B, albeit rare in human populations, are among the strongest genetic risk factors for SLE or lupus-like disease, across HLA haplotypes and racial backgrounds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_assertion evidence source_evidence_literature NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_assertion SIO_000772 14719377 NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_assertion wasDerivedFrom befree-20140225 NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_assertion wasGeneratedBy ECO_0000203 NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340778.RAq2tABTeLaEaM9s6kAZS3nevJmUZ3vt4mFsQEDd7uWwY130_provenance.