Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_assertion description "[DRB1*0301 was a common genetic risk factor for familial and sporadic IIM, but contributed less to the genetic risk of familial IIM (etiologic fraction 0.35 versus 0.51 in sporadic IIM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_assertion evidence source_evidence_literature NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_assertion SIO_000772 9550481 NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_assertion wasDerivedFrom befree-20150227 NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_assertion wasGeneratedBy ECO_0000203 NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP456194.RAeqrXjuR6R-xHA1aEer0JtHuiFwIBYXteRd1XAyHrFFw130_provenance.