hgug4110bOMIM           package:hgug4110b           R Documentation

_M_a_p _b_e_t_w_e_e_n _M_a_n_u_f_a_c_t_u_r_e_r _I_d_e_n_t_i_f_i_e_r_s _a_n_d _M_e_n_d_e_l_i_a_n _I_n_h_e_r_i_t_a_n_c_e _i_n
_M_a_n (_M_I_M) _i_d_e_n_t_i_f_i_e_r_s

_D_e_s_c_r_i_p_t_i_o_n:

     hgug4110bOMIM is an R environment that provides mappings between
     manufacturer ids and OMIM ids.

_D_e_t_a_i_l_s:

     Each manufacturer id is mapped to a vector of OMIM ids. The vector
     length may be one or longer, depending on how many OMIM ids the
     manufacturer id maps to. An 'NA' is reported for any manufacturer
     id that cannot be mapped to an OMIM id at this time.

     OMIM is based upon the book Mendelian Inheritance in Man (V. A.
     McKusick) and focuses primarily on inherited or heritable genetic
     diseases. It contains textual information, pictures, and reference
     information that can be searched using various terms, among which
     the MIM number is one. 

     Mappings were based on data provided by:

     Entrez Gene:<URL:
     http://gopher5/compbio/annotationSourceData/ftp.ncbi.nlm.nih.gov/g
     ene/DATA/>. Built: Source data downloaded from Entrez Gene on Tue
     May 17 14:10:10 2005

     Package built Tue May 17 14:20:05 2005

_R_e_f_e_r_e_n_c_e_s:

     <URL: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene> <URL:
     http://www3.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM>

_E_x_a_m_p_l_e_s:

         # Convert the environment to a list
         xx <- as.list(hgug4110bOMIM)
         # Remove probe ids that do not map to any MIM number
         xx <- xx[!is.na(xx)]
         if(length(xx) > 0){
             # The MIM numbers for the first two elements of XX
             xx[1:2]
             # Get the first one
             xx[[1]]
         }

