Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_assertion> ?p ?o ?g. }
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- NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_assertion type Assertion NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_head.
- NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_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." NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_provenance.
- NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_assertion evidence source_evidence_literature NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_provenance.
- NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_assertion SIO_000772 19414860 NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_provenance.
- NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_assertion wasDerivedFrom gad-20150221 NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_provenance.
- NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_assertion wasGeneratedBy ECO_0000203 NP87219.RAhW_EusQLbOfpQ3TgmMwNxAkt4XH20cBw88pI4M596mE130_provenance.