Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion type Assertion NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_head.
- NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion description "[FVII deficiency in both populations is caused by a founder A244V mutation in the F7 gene and DJS is caused by two founder mutations, I1173F and R1150H in the MRP2 gene that are specific for Iranian and Moroccan Jewish patients, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_provenance.
- NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion evidence source_evidence_literature NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_provenance.
- NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion SIO_000772 17287630 NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_provenance.
- NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion wasDerivedFrom befree-20150227 NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_provenance.
- NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_assertion wasGeneratedBy ECO_0000203 NP318189.RASemSB0xSgbFWeA-a0ONveOymgt_vvXw3nnfSorWUNpA130_provenance.