Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion> ?p ?o ?g. }
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- NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion type Assertion NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_head.
- NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion description "[Here we show that an N-ethyl-N-nitrosourea-induced nonsense mutation of Cd36 (oblivious) causes a recessive immunodeficiency phenotype in which macrophages are insensitive to the R-enantiomer of MALP-2 (a diacylated bacterial lipopeptide) and to lipoteichoic acid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_provenance.
- NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion evidence source_evidence_curated NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_provenance.
- NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion SIO_000772 15690042 NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_provenance.
- NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion wasDerivedFrom ctd_human-20150221 NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_provenance.
- NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_assertion wasGeneratedBy ECO_0000218 NP9689.RABC2EM8BO3JSO3yxeB6b32dOjzrlK9UYHxL9BQBmc_eo130_provenance.