Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_assertion description "[We suggest that alleles DQB1*04 may be involved in the genetic susceptibility of PR based on the significant predominance of those alleles observed in the black PR patients. We also recommend that more studies are conducted on populations of other ethnic ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_assertion evidence source_evidence_literature NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_assertion SIO_000772 16405603 NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_assertion wasDerivedFrom gad-20150221 NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_assertion wasGeneratedBy ECO_0000203 NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.
- gad-20150221 importedOn "2015-02-21" NP98413.RAHsQkepfCjDp5oUxvGxJWG5i4UD1vfBaTUl0_PL91e5Q130_provenance.