Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_assertion description "[No effects of MTHFR C677T polymorphism on CIN II/III risk and MTHFR A1298C or MS A2756G polymorphisms on cervical cancer risk were detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_assertion evidence source_evidence_literature NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_assertion SIO_000772 23864153 NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_assertion wasDerivedFrom befree-20150227 NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_assertion wasGeneratedBy ECO_0000203 NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP575739.RAflVyvxiFHULekynp0zzriRHvAV3tIGr5W9gRtMaH_yE130_provenance.