Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion type Assertion NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_head.
- NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion description "[Patients homozygous for the W1282X mutation (n = 16) and patients heterozygous for the delta F508 and W1282X mutations (n = 22) had similarly severe disease, reflected by pancreatic insufficiency, high incidence of meconium ileus (37% and 27%, respectively), early age at diagnosis, poor nutritional status, and variable pulmonary function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_provenance.
- NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion evidence source_evidence_literature NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_provenance.
- NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion SIO_000772 1370365 NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_provenance.
- NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion wasDerivedFrom befree-20140225 NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_provenance.
- NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_assertion wasGeneratedBy ECO_0000203 NP492332.RA-N8gC7daz5LtNYluFdKahxFbQqopienUFN0WgyK9GvI130_provenance.