Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_assertion description "[It is concluded that genetic variants of the TNFA gene may affect the risk of CRS in a clinically well-defined group of CRSNP(+)ASA(+) patients in the Hungarian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_assertion evidence source_evidence_literature NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_assertion SIO_000772 23446846 NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_assertion wasDerivedFrom befree-2016 NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_assertion wasGeneratedBy ECO_0000203 NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1056511.RA_yMcsLfrWpsAeDdVa2tXTp4sxelewQCWZX6Y0SV-sT4130_provenance.