Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion type Assertion NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_head.
- NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion description "[It is noteworthy that genetic variants in CASP8 were associated with risk of all major NHL subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_provenance.
- NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion evidence source_evidence_literature NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_provenance.
- NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion SIO_000772 19414860 NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_provenance.
- NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion wasDerivedFrom befree-2016 NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_provenance.
- NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_assertion wasGeneratedBy ECO_0000203 NP736525.RAIx93QNLGmvp8bV_ip0i4580vblAMgqQNTwDuTMqfS-U130_provenance.