PubDictionaries

OMIM in Bio2RDF r.3

53,354 entries

Label	Id

NEMALINE MYOPATHY 10	http://bio2rdf.org/omim_resource:616112_allele_1
NEMALINE MYOPATHY 10	http://bio2rdf.org/omim_resource:616112_allele_0
Myokymia (in some patients)	http://bio2rdf.org/omim_resource:d433076f5d40d882ab5ece252a92418d
Myoclonus, action	http://bio2rdf.org/omim_resource:b4268081a64f4f29460fd3b97b338294
Myoclonic-astatic seizures	http://bio2rdf.org/omim_resource:2c742211924b4654f0b23303117db14f
Myoclonic epilepsy, refractory	http://bio2rdf.org/omim_resource:9e238a93d321ac06125c49cc5f18c834
Myasthenia	http://bio2rdf.org/omim_resource:0048a872d639a0171740f3a2a03823d6
Muscle weakness, mainly proximal	http://bio2rdf.org/omim_resource:56b25851556040fd03dcd759ff1d8b6d
Muscle atrophy, severe	http://bio2rdf.org/omim_resource:155a8aa8e4a5d21e39c37a675514823d
Mottled pigmentation of retina	http://bio2rdf.org/omim_resource:8e129a700859c6dfefe6efa26566e2d5
Motor neuropathy (1 family)	http://bio2rdf.org/omim_resource:a3d6d1bf17f463dae93bd05e04420bf6
Motor development delay (83%)	http://bio2rdf.org/omim_resource:da9a20aebe911be257255855e7f5c18f
Moderate-low complement C3	http://bio2rdf.org/omim_resource:4a408fb59ea3081808b9afc0614e09c7
Mitral valve hypoplasia	http://bio2rdf.org/omim_resource:eeb47d62bebb7e336e37d57c382a6ba7
Mild thoracic kyphosis	http://bio2rdf.org/omim_resource:ee18b923eb37dee2861a30b0a80c5de2