Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion type Assertion NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_head.
- NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion description "[A point mutation responsible for human erythrocyte AMP deaminase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_provenance.
- NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion evidence source_evidence_curated NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_provenance.
- NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion SIO_000772 8004104 NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_provenance.
- NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion wasDerivedFrom uniprot-2016 NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_provenance.
- NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_assertion wasGeneratedBy ECO_0000218 NP8682.RAT9Y-QfL0uhVfFk1T4Vy3C2GThDp_JGT5YbWRwOPDW-0130_provenance.