Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_assertion description "[the 1672T variant of the OCTN1 gene and the -207C variant of the OCTN2 gene represent risk factors for Crohn disease in the Greek population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_assertion evidence source_evidence_literature NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_assertion SIO_000772 16437728 NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_assertion wasDerivedFrom lhgdn-20090331 NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_assertion wasGeneratedBy ECO_0000203 NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP136320.RA6HAyrAjbv3F3Zt78NYjM7D3efXwlQ2MSHAl5Lm83ZwQ130_provenance.