Bio/Phenotype/OMIM/OMIMentry.pm | |||
---|---|---|---|
Criterion | Covered | Total | % |
subroutine | 29 | 32 | 90.6 |
pod | 21 | 23 | 91.3 |
line | count | pod | subroutine |
---|---|---|---|
97 | 2 | n/a | BEGIN |
99 | 2 | n/a | BEGIN |
100 | 2 | n/a | BEGIN |
102 | 2 | n/a | BEGIN |
103 | 2 | n/a | BEGIN |
104 | 2 | n/a | BEGIN |
106 | 2 | n/a | BEGIN |
140 | 3 | Yes | new |
214 | 6 | Yes | init |
251 | 1 | No | to_string |
317 | 13 | Yes | MIM_number |
350 | 13 | Yes | title |
374 | 13 | Yes | alternative_titles_and_symbols |
403 | 12 | Yes | more_than_two_genes |
437 | 12 | Yes | is_separate |
464 | 13 | Yes | mapping_method |
491 | 13 | Yes | gene_status |
532 | 9 | Yes | clinical_symptoms |
557 | 8 | Yes | clinical_symptoms_raw |
575 | 0 | Yes | add_clinical_symptoms |
596 | 0 | Yes | query_clinical_symptoms |
602 | 0 | No | get_clinical_symptom_organs |
619 | 13 | Yes | created |
641 | 13 | Yes | contributors |
663 | 13 | Yes | edited |
686 | 11 | Yes | additional_references |
707 | 13 | Yes | miniMIM |
729 | 16 | Yes | each_AllelicVariant |
750 | 3 | Yes | add_AllelicVariants |
775 | 8 | Yes | remove_AllelicVariants |
789 | 5 | n/a | _array_to_string |
821 | 16 | n/a | _is_true_or_false |