Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_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 origins, preferentially with higher resolution techniques of DNA typing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_assertion evidence source_evidence_literature NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_assertion SIO_000772 16405603 NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_assertion wasDerivedFrom gad-20130706 NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_assertion wasGeneratedBy ECO_0000203 NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64969.RAlTEO81fyPpA5wb4u3mNKn2QtOCTK8Ql8tNatSB5v4z8130_provenance.